GoConqr has a new look! Let us know what you think.

Sign up free

Flashcards

SYNDROMES

Khu gh English 105 cards

APERT SYNDROME - MR - MITTEN HANDS - PARROT NOSE - HIGH NARROW PALATE - CROWDING - SUPERNUMERARY - ECTOPIC ERUPTION "AH…

Cards in this deck (105)

  1. 1—APERT SYNDROME
    - MR
    - MITTEN HANDS
    - PARROT NOSE
    - HIGH NARROW PALATE
    - CROWDING
    - SUPERNUMERARY
    - ECTOPIC ERUPTION
    "AH PAIR OF MITTENS"    APERT SYNDROME - MR - MITTEN HANDS - PARROT NOSE - HIGH NARROW PALATE - CROWDING - SUPERNUMERARY - ECTOPIC ERUPTION "AH PAIR OF MITTENS"
  2. 2—APERT SYNDROME
    - MR
    - MITTEN HANDS
    - PARROT NOSE
    - HIGH NARROW PALATE
    - CROWDING
    - SUPERNUMERARY
    - ECTOPIC ERUPTION
    "AH PAIR OF MITTENS"    APERT SYNDROME - MR - MITTEN HANDS - PARROT NOSE - HIGH NARROW PALATE - CROWDING - SUPERNUMERARY - ECTOPIC ERUPTION "AH PAIR OF MITTENS"
  3. 3—APERT SYNDROME
    - MR
    - MITTEN HANDS
    - PARROT NOSE
    - HIGH NARROW PALATE
    - CROWDING
    - SUPERNUMERARY
    - ECTOPIC ERUPTION
    "AH PAIR OF MITTENS"    APERT SYNDROME - MR - MITTEN HANDS - PARROT NOSE - HIGH NARROW PALATE - CROWDING - SUPERNUMERARY - ECTOPIC ERUPTION "AH PAIR OF MITTENS"
  4. 4—CARPENTER
    - PARTIAL SYNDACTYLY
    - CARIAC ABNORMALITIES
    - ACROCEPHALY
    - OBESITY    CARPENTER - PARTIAL SYNDACTYLY - CARIAC ABNORMALITIES - ACROCEPHALY - OBESITY
  5. 5—PFIEFFER SYNDROME
    - NORMAL INTELLIGENCE
    - BROAD THUMB AND GREAT TOES
    - EXOPTHALMOS    PFIEFFER SYNDROME - NORMAL INTELLIGENCE - BROAD THUMB AND GREAT TOES - EXOPTHALMOS
  6. 6—PFIEFFER SYNDROME
    - NORMAL INTELLIGENCE
    - BROAD THUMB AND GREAT TOES
    - EXOPTHALMOS    PFIEFFER SYNDROME - NORMAL INTELLIGENCE - BROAD THUMB AND GREAT TOES - EXOPTHALMOS
  7. 7—APERT SYNDROME
    - MR
    - MITTEN HANDS
    - PARROT NOSE
    - HIGH NARROW PALATE
    - CROWDING
    - SUPERNUMERARY
    - ECTOPIC ERUPTION
    "AH PAIR OF MITTENS"    APERT SYNDROME - MR - MITTEN HANDS - PARROT NOSE - HIGH NARROW PALATE - CROWDING - SUPERNUMERARY - ECTOPIC ERUPTION "AH PAIR OF MITTENS"
  8. 8—APERT SYNDROME
    - MR
    - MITTEN HANDS
    - PARROT NOSE
    - HIGH NARROW PALATE
    - CROWDING
    - SUPERNUMERARY
    - ECTOPIC ERUPTION
    "AH PAIR OF MITTENS"    APERT SYNDROME - MR - MITTEN HANDS - PARROT NOSE - HIGH NARROW PALATE - CROWDING - SUPERNUMERARY - ECTOPIC ERUPTION "AH PAIR OF MITTENS"
  9. 9—CROUZON SYNDROME
    - NO HAND ABNORMALITIES
    - NORMAL INTELLIGENCE
    - CROWDED
    - INVERTED V SHAPED PALATE
    - HYPO AND HYPERDONTIA
    - MACRO AND MICRODONTIA
    "HEY I HAVE NORMAL INTELLIGENCE AND NORMAL HANDS, I SHOULD MAKE SOME CROUTONS"    CROUZON SYNDROME - NO HAND ABNORMALITIES - NORMAL INTELLIGENCE - CROWDED - INVERTED V SHAPED PALATE - HYPO AND HYPERDONTIA - MACRO AND MI...
  10. 10—CROUZON SYNDROME
    - NO HAND ABNORMALITIES
    - NORMAL INTELLIGENCE
    - CROWDED
    - INVERTED V SHAPED PALATE
    - HYPO AND HYPERDONTIA
    - MACRO AND MICRODONTIA
    "HEY I HAVE NORMAL INTELLIGENCE AND NORMAL HANDS, I SHOULD MAKE SOME CROUTONS"    CROUZON SYNDROME - NO HAND ABNORMALITIES - NORMAL INTELLIGENCE - CROWDED - INVERTED V SHAPED PALATE - HYPO AND HYPERDONTIA - MACRO AND MI...
  11. 11—ACHONDROPLASIA
    - MOST COMMON TYPE OF DWARFISM
    - SHORT, SHORT ARMS
    - SHORT LEGS
    - TRIDENT HANDS
    - HYPODONTIA
    - LORDOSIS    ACHONDROPLASIA - MOST COMMON TYPE OF DWARFISM - SHORT, SHORT ARMS - SHORT LEGS - TRIDENT HANDS - HYPODONTIA - LORDOSIS
  12. 12—ACHONDROPLASIA
    - MOST COMMON TYPE OF DWARFISM
    - SHORT, SHORT ARMS
    - SHORT LEGS
    - TRIDENT HANDS
    - HYPODONTIA
    - LORDOSIS    ACHONDROPLASIA - MOST COMMON TYPE OF DWARFISM - SHORT, SHORT ARMS - SHORT LEGS - TRIDENT HANDS - HYPODONTIA - LORDOSIS
  13. 13—ACHONDROPLASIA
    - MOST COMMON TYPE OF DWARFISM
    - SHORT, SHORT ARMS
    - SHORT LEGS
    - TRIDENT HANDS
    - HYPODONTIA
    - LORDOSIS    ACHONDROPLASIA - MOST COMMON TYPE OF DWARFISM - SHORT, SHORT ARMS - SHORT LEGS - TRIDENT HANDS - HYPODONTIA - LORDOSIS
  14. 14—ACHONDROPLASIA
    - MOST COMMON TYPE OF DWARFISM
    - SHORT, SHORT ARMS
    - SHORT LEGS
    - TRIDENT HANDS
    - HYPODONTIA
    - LORDOSIS    ACHONDROPLASIA - MOST COMMON TYPE OF DWARFISM - SHORT, SHORT ARMS - SHORT LEGS - TRIDENT HANDS - HYPODONTIA - LORDOSIS
  15. 15—ELLIS-VAN CREVALD
    - AKA CHONDROECTODERMAL DYSPLASIA
    - POLYDACTYLY
    - SHORT
    - NATAL AND CONICAL TEETH
    - CARDIAC DEFECTS
    - ABSENT MAXILLARY SULCUS    ELLIS-VAN CREVALD - AKA CHONDROECTODERMAL DYSPLASIA - POLYDACTYLY - SHORT - NATAL AND CONICAL TEETH - CARDIAC DEFECTS - ABSENT MAXILLARY ...
  16. 16—ELLIS-VAN CREVALD
    - AKA CHONDROECTODERMAL DYSPLASIA
    - POLYDACTYLY
    - SHORT
    - NATAL AND CONICAL TEETH
    - CARDIAC DEFECTS
    - ABSENT MAXILLARY SULCUS    ELLIS-VAN CREVALD - AKA CHONDROECTODERMAL DYSPLASIA - POLYDACTYLY - SHORT - NATAL AND CONICAL TEETH - CARDIAC DEFECTS - ABSENT MAXILLARY ...
  17. 17—HALLERMAN-STREIFF
    - SHORT
    - Beak Nose
    - SMALL PALPEBRAL FISSURES
    - BILATERAL CATARACTS
    - NATAL TEETH
    - DYSCEPHALY
    - HYPOTRICHOSIS (LACK OF HAIR)    HALLERMAN-STREIFF - SHORT - Beak Nose - SMALL PALPEBRAL FISSURES - BILATERAL CATARACTS - NATAL TEETH - DYSCEPHALY - HYPOTRICHOSIS (LACK O...
  18. 18—HALLERMAN-STREIFF
    - SHORT
    - SMALL PALPEBRAL FISSURES
    - BILATERAL CATARACTS
    - NATAL TEETH
    - DYSCEPHALY
    - HYPOTRICHOSIS (LACK OF HAIR)    HALLERMAN-STREIFF - SHORT - SMALL PALPEBRAL FISSURES - BILATERAL CATARACTS - NATAL TEETH - DYSCEPHALY - HYPOTRICHOSIS (LACK OF HAIR)
  19. 19—HALLERMAN-STREIFF
    - SHORT
    - SMALL PALPEBRAL FISSURES
    - BILATERAL CATARACTS
    - NATAL TEETH
    - DYSCEPHALY
    - HYPOTRICHOSIS (LACK OF HAIR)    HALLERMAN-STREIFF - SHORT - SMALL PALPEBRAL FISSURES - BILATERAL CATARACTS - NATAL TEETH - DYSCEPHALY - HYPOTRICHOSIS (LACK OF HAIR)
  20. 20—MPS 1: HURLER SYNDROME
    - COARSE FACIES
    - DWARFISM
    - SEVERE ID
    - OPEN MOUTH
    - PROTRUDING TONGUE,
    - ENLARGED DENTAL FOLLICLE    MPS 1: HURLER SYNDROME - COARSE FACIES - DWARFISM - SEVERE ID - OPEN MOUTH - PROTRUDING TONGUE, - ENLARGED DENTAL FOLLICLE
  21. 21—MPS 1: HURLER SYNDROME
    - COARSE FACIES
    - DWARFISM
    - SEVERE ID
    - OPEN MOUTH
    - PROTRUDING TONGUE,
    - ENLARGED DENTAL FOLLICLE    MPS 1: HURLER SYNDROME - COARSE FACIES - DWARFISM - SEVERE ID - OPEN MOUTH - PROTRUDING TONGUE, - ENLARGED DENTAL FOLLICLE
  22. 22—MPS 1: HURLER SYNDROME
    - COARSE FACIES
    - DWARFISM
    - SEVERE ID
    - OPEN MOUTH
    - PROTRUDING TONGUE,
    - ENLARGED DENTAL FOLLICLE    MPS 1: HURLER SYNDROME - COARSE FACIES - DWARFISM - SEVERE ID - OPEN MOUTH - PROTRUDING TONGUE, - ENLARGED DENTAL FOLLICLE
  23. 23—MPS 1: HURLER SYNDROME
    - COARSE FACIES
    - DWARFISM
    - SEVERE ID
    - OPEN MOUTH
    - PROTRUDING TONGUE,
    - ENLARGED DENTAL FOLLICLE    MPS 1: HURLER SYNDROME - COARSE FACIES - DWARFISM - SEVERE ID - OPEN MOUTH - PROTRUDING TONGUE, - ENLARGED DENTAL FOLLICLE
  24. 24—MPS II: HUNTER
    - LATER ONSET
    - X-LINKED RECESSIVE
    - DWARFISM
    - DEAFNESS
    - PALPULAR LESIONS ON SCAPULA, LATERAL ARMS AND THIGHS
    - DELAYED PRIMARY EXFOLIATION AND PERMANENT ERUPTION
    - COARSE FACIES    MPS II: HUNTER - LATER ONSET - X-LINKED RECESSIVE - DWARFISM - DEAFNESS - PALPULAR LESIONS ON SCAPULA, LATERAL ARMS AND THIGHS - DELAYED ...
  25. 25—OSTEOGENESIS IMPERFECTA
    - AD
    - DI SHIELDS 1
    - BLUE SCLERA
    - LOOSE LIGAMENTS
    - BOWED LEGS
    - FRAGILE BONES
    - MACROCEPHALY    OSTEOGENESIS IMPERFECTA - AD - DI SHIELDS 1 - BLUE SCLERA - LOOSE LIGAMENTS - BOWED LEGS - FRAGILE BONES - MACROCEPHALY
  26. 26—TURNER SYNDROME
    - GONADAL DYSGENESIS
    - 45 X KARYOTYPE
    - SHORT
    - AMENORRHEA
    - CV DEFECT (COARCTATION OF AORTA)
    - WEBBED NECK
    - NORMAL IQ
    - ENAMEL HYPOPLASIA    TURNER SYNDROME - GONADAL DYSGENESIS - 45 X KARYOTYPE - SHORT - AMENORRHEA - CV DEFECT (COARCTATION OF AORTA) - WEBBED NECK - NORMAL IQ -...
  27. 27—TURNER SYNDROME
    - GONADAL DYSGENESIS
    - 45 X KARYOTYPE
    - SHORT
    - AMENORRHEA
    - CV DEFECT (COARCTATION OF AORTA)
    - WEBBED NECK
    - NORMAL IQ
    - ENAMEL HYPOPLASIA    TURNER SYNDROME - GONADAL DYSGENESIS - 45 X KARYOTYPE - SHORT - AMENORRHEA - CV DEFECT (COARCTATION OF AORTA) - WEBBED NECK - NORMAL IQ -...
  28. 28—TURNER SYNDROME
    - GONADAL DYSGENESIS
    - 45 X KARYOTYPE
    - SHORT
    - AMENORRHEA
    - CV DEFECT (COARCTATION OF AORTA)
    - WEBBED NECK
    - NORMAL IQ
    - ENAMEL HYPOPLASIA    TURNER SYNDROME - GONADAL DYSGENESIS - 45 X KARYOTYPE - SHORT - AMENORRHEA - CV DEFECT (COARCTATION OF AORTA) - WEBBED NECK - NORMAL IQ -...
  29. 29—CHERUBISM
    - BILATERAL CHEEK SWELLING
    - MULTILOCULAR RLs (SIMILAR TO CENTRAL GIANT CELL GRANULOMA)    CHERUBISM - BILATERAL CHEEK SWELLING - MULTILOCULAR RLs (SIMILAR TO CENTRAL GIANT CELL GRANULOMA)
  30. 30—CHERUBISM
    - BILATERAL CHEEK SWELLING
    - MULTILOCULAR RLs (SIMILAR TO CENTRAL GIANT CELL GRANULOMA)    CHERUBISM - BILATERAL CHEEK SWELLING - MULTILOCULAR RLs (SIMILAR TO CENTRAL GIANT CELL GRANULOMA)
  31. 31—FIBROUS DYSPLASIA - MONOCYSTIC
    - BENIGN FIBROUS OSSEOUS LESIONS OF JAW
    - ENLARGEMENT OF JAW
    - MAXILLA
    - GROUND GLASS
    - OBLITERATED MUCOBUCCAL FOLD    FIBROUS DYSPLASIA - MONOCYSTIC - BENIGN FIBROUS OSSEOUS LESIONS OF JAW - ENLARGEMENT OF JAW - MAXILLA - GROUND GLASS - OBLITERATED MUCOBU...
  32. 32—MCCUNE ALBRIGHT - FIBROUS DYSPLASIA POLYOSTOTIC
    - ABNORMAL PIGMENTATION (CAFE-AU-LAIT - "COAST OF MAINE")
    - GROUND GLASS
    - HYPERTHYROID
    - HYPERPARATHYROID
    - PRECOCIOUS PUBERTY    MCCUNE ALBRIGHT - FIBROUS DYSPLASIA POLYOSTOTIC - ABNORMAL PIGMENTATION (CAFE-AU-LAIT - "COAST OF MAINE") - GROUND GLASS - HYPERTHYROID -...
  33. 33—GARDENER
    - MULTIPLE INTESTINAL POLYPS
    - MULTIPLE OSTEOMAS OF JAW
    - PERIAPICAL MIXED RL/ROs    GARDENER - MULTIPLE INTESTINAL POLYPS - MULTIPLE OSTEOMAS OF JAW - PERIAPICAL MIXED RL/ROs
  34. 34—GARDENER
    - MULTIPLE INTESTINAL POLYPS
    - MULTIPLE OSTEOMAS OF JAW
    - PERIAPICAL MIXED RL/ROs    GARDENER - MULTIPLE INTESTINAL POLYPS - MULTIPLE OSTEOMAS OF JAW - PERIAPICAL MIXED RL/ROs
  35. 35—GOLDENHAR (HEMIFACIAL MICROSOMIA)
    - TRIAD: FACIAL ASYMMETRY, EAR AND/OR EYE MALFORMATION, VERTEBRAL ANOMALIES
    - UNILATERAL
    - CARIAC DEFECTS!! VSD PDA
    - MICROTIA
    - MACROSTOMIA
    - MICRODONTIA
    - FAILURE OF FORMATION OF RAMUS AND CONDYLE    GOLDENHAR (HEMIFACIAL MICROSOMIA) - TRIAD: FACIAL ASYMMETRY, EAR AND/OR EYE MALFORMATION, VERTEBRAL ANOMALIES - UNILATERAL - CARIAC DEFEC...
  36. 36—GOLDENHAR (HEMIFACIAL MICROSOMIA)
    - TRIAD: FACIAL ASYMMETRY, EAR AND/OR EYE MALFORMATION, VERTEBRAL ANOMALIES
    - UNILATERAL
    - CARIAC DEFECTS
    - MICROTIA
    - MACROSTOMIA
    - MICRODONTIA
    - FAILURE OF FORMATION OF RAMUS AND CONDYLE    GOLDENHAR (HEMIFACIAL MICROSOMIA) - TRIAD: FACIAL ASYMMETRY, EAR AND/OR EYE MALFORMATION, VERTEBRAL ANOMALIES - UNILATERAL - CARIAC DEFEC...
  37. 37—HEMIFACIAL HYPERTROPHY
    - ENLARGEMENT OF HEAD AND TEETH EVIDENT AT BIRTH
    - EMBRYONAL TUMOR (WILMS)    HEMIFACIAL HYPERTROPHY - ENLARGEMENT OF HEAD AND TEETH EVIDENT AT BIRTH - EMBRYONAL TUMOR (WILMS)
  38. 38—HEMIFACIAL HYPERTROPHY
    - ENLARGEMENT OF HEAD AND TEETH EVIDENT AT BIRTH
    - EMBRYONAL TUMOR (WILMS)
    - TEETH MAY EXFOLIATE AND ERUPTION EARLY    HEMIFACIAL HYPERTROPHY - ENLARGEMENT OF HEAD AND TEETH EVIDENT AT BIRTH - EMBRYONAL TUMOR (WILMS) - TEETH MAY EXFOLIATE AND ERUPTION EARLY
  39. 39CAUSES OF CL AND CP- MATERNAL ALCOHOL AND CIGARETTE USE
    - FOLIC ACID DEFICIENCY
    - CORTICOSTEROID USE
    - ANTICONVULSANT USE
  40. 40CONDITIONS WITH CL AND CP- CLEIDOCRANIAL DYSOSTOSIS
    - ORAL-FACIAL-DIGITAL SYNDROME
    - PIERRE ROBBIN SEQUENCE
    - TREACHER COLLINS SYNDROME
  41. 41—CLEIDOCRANIAL DYSPLASIA (CLEIDOCRANIAL DYSOSTOSIS)
    - CLAVICLE DEFECT
    - FRONTAL BOSSING
    - BRACHYCEPHALY
    - HIGH PALATE
    - SUPERNUMERARY
    - DELAYED EXFOLIATION AND ERUPTION
    - ROOTS LACK CELLULAR CEMENTUM    CLEIDOCRANIAL DYSPLASIA (CLEIDOCRANIAL DYSOSTOSIS) - CLAVICLE DEFECT - FRONTAL BOSSING - BRACHYCEPHALY - HIGH PALATE - SUPERNUMERARY - DE...
  42. 42—CLEIDOCRANIAL DYSPLASIA (CLEIDOCRANIAL DYSOSTOSIS)
    - CLAVICLE DEFECT
    - BRACHYCEPHALY
    - FRONTAL BOSSING
    - HIGH PALATE
    - SUPERNUMERARY
    - DELAYED EXFOLIATION AND ERUPTION
    - ROOTS LACK CELLULAR CEMENTUM    CLEIDOCRANIAL DYSPLASIA (CLEIDOCRANIAL DYSOSTOSIS) - CLAVICLE DEFECT - BRACHYCEPHALY - FRONTAL BOSSING - HIGH PALATE - SUPERNUMERARY - DE...
  43. 43—CLEIDOCRANIAL DYSPLASIA (CLEIDOCRANIAL DYSOSTOSIS)
    - CLAVICLE DEFECT
    - BRACHYCEPHALY
    - FRONTAL BOSSING
    - HIGH PALATE
    - SUPERNUMERARY
    - DELAYED EXFOLIATION AND ERUPTION
    - ROOTS LACK CELLULAR CEMENTUM    CLEIDOCRANIAL DYSPLASIA (CLEIDOCRANIAL DYSOSTOSIS) - CLAVICLE DEFECT - BRACHYCEPHALY - FRONTAL BOSSING - HIGH PALATE - SUPERNUMERARY - DE...
  44. 44—ORO-FACIAL-DIGITAL SYNDROME
    - MR
    - SYNDACTYLY
    - CLINODACTYLY (CURVED FINGERS)
    - HYPOTRICHOSIS
    - BRACHYCEPHALY
    - CLEFT TONGUE AND PALATE
    PSEUDO CLEFT LIP
    - MULTIPLE HYPERPLASTIC FRENA WITH CLEFT
    - HYPO (MAND LATERALS)
    - HYPER (MAX CANINES)
    -    ORO-FACIAL-DIGITAL SYNDROME - MR - SYNDACTYLY - CLINODACTYLY (CURVED FINGERS) - HYPOTRICHOSIS - BRACHYCEPHALY - CLEFT TONGUE AND PALATE P...
  45. 45—ORO-FACIAL-DIGITAL SYNDROME
    - MR
    - SYNDACTYLY
    - CLINOSYNDACTYLY (CURVED FINGERS)
    - HYPOTRICHOSIS
    - CLEFT TONGUE AND PALATE
    - PSEUDO CLEFT LIP
    - MULTIPLE HYPERPLASTIC FRENA WITH CLEFT
    - HYPO (MAND LATERALS)
    - HYPER (MAX CANINES)    ORO-FACIAL-DIGITAL SYNDROME - MR - SYNDACTYLY - CLINOSYNDACTYLY (CURVED FINGERS) - HYPOTRICHOSIS - CLEFT TONGUE AND PALATE - PSEUDO CLEFT...
  46. 46—PIERRE-ROBIN SEQUENCE
    - Micrognathia
    - Glossoptosis
    - Cleft Palate
    - U-shaped Cleft
    - Cardiac Defect    PIERRE-ROBIN SEQUENCE - Micrognathia - Glossoptosis - Cleft Palate - U-shaped Cleft - Cardiac Defect
  47. 47—PIERRE-ROBIN SEQUENCE
    - Micrognathia
    - Glossoptosis
    - Cleft Palate
    - U-shaped Cleft
    - Cardiac Defect    PIERRE-ROBIN SEQUENCE - Micrognathia - Glossoptosis - Cleft Palate - U-shaped Cleft - Cardiac Defect
  48. 48—TREACHER COLLINS SYNDROME
    - LARGE FISHLIKE MOUTH
    - DOWNSLOPING PALPEBRAL FISSURES
    - DEPRESSED CHEEK BONES
    - HYPOPLASTIC MANDIBLE
    - CLEFT PALATE
    - DEFORMED PINNAE
    - ENAMEL HYPOPLASIA
    - NORMAL INTELLIGENCE    TREACHER COLLINS SYNDROME - LARGE FISHLIKE MOUTH - DOWNSLOPING PALPEBRAL FISSURES - DEPRESSED CHEEK BONES - HYPOPLASTIC MANDIBLE - CLEFT ...
  49. 49—TREACHER COLLINS SYNDROME
    - LARGE FISHLIKE MOUTH
    - DOWNSLOPING PALPEBRAL FISSURES
    - DEPRESSED CHEEK BONES
    - HYPOPLASTIC MANDIBLE
    - CLEFT PALATE
    - DEFORMED PINNAE
    - ENAMEL HYPOPLASIA
    - NORMAL INTELLIGENCE    TREACHER COLLINS SYNDROME - LARGE FISHLIKE MOUTH - DOWNSLOPING PALPEBRAL FISSURES - DEPRESSED CHEEK BONES - HYPOPLASTIC MANDIBLE - CLEFT ...
  50. 50—TREACHER COLLINS SYNDROME
    - LARGE FISH LIKE MOUTH
    - DOWNSLOPING PALPEBRAL FISSURES
    - DEPRESSED CHEEK BONES
    - HYPOPLASTIC MANDIBLE
    - CLEFT PALATE
    - DEFORMED PINNAE
    - ENAMEL HYPOPLASIA
    - NORMAL INTELLIGENCE    TREACHER COLLINS SYNDROME - LARGE FISH LIKE MOUTH - DOWNSLOPING PALPEBRAL FISSURES - DEPRESSED CHEEK BONES - HYPOPLASTIC MANDIBLE - CLEFT...
  51. 51—VAN DER WOUDE
    - MOST COMMON SYNDROME ASSOCIATED WITH CLEFT LIP AND PALATE
    - LIP PITS
    - HYPODONTIA/ ANODONTIA    VAN DER WOUDE - MOST COMMON SYNDROME ASSOCIATED WITH CLEFT LIP AND PALATE - LIP PITS - HYPODONTIA/ ANODONTIA
  52. 52—PHACE SYNDROME
    - LARGE HEMANGIOMA
    - BRAIN MALFORMATION
    - CARDIAC ABNORMALITIES
    - EYE ABNORMALITIES    PHACE SYNDROME - LARGE HEMANGIOMA - BRAIN MALFORMATION - CARDIAC ABNORMALITIES - EYE ABNORMALITIES
  53. 53—HECK'S DZ
    - PINK, WHITE NODULES
    - BUCCAL/LABIAL MUCOSA, ANTERIOR TONGUE, GINGIVA    HECK'S DZ - PINK, WHITE NODULES - BUCCAL/LABIAL MUCOSA, ANTERIOR TONGUE, GINGIVA
  54. 54—NEUROFIBROMATOSIS
    - CAFE-AU-LAIT SPOTS
    - ENLARGED FUNGIFORM PAPILLA
    - WIDENED IAN CANAL
    - ORAL FIBROMAS
    - LISCH NODULES
    - SUBCUTANEOUS NEUROFIBROMAS    NEUROFIBROMATOSIS - CAFE-AU-LAIT SPOTS - ENLARGED FUNGIFORM PAPILLA - WIDENED IAN CANAL - ORAL FIBROMAS - LISCH NODULES - SUBCUTANEOUS NE...
  55. 55—EHLERS DANLOS
    - HYPERMOBILITY
    - SUBLUX OF TMJ
    - GORLIN SIGN    EHLERS DANLOS - HYPERMOBILITY - SUBLUX OF TMJ - GORLIN SIGN
  56. 56—HYPOPHOSPHOTASIA
    - LACK OF SERUM ALKALINE PHOSPHATASE
    - LITTLE CEMENTUM PRODUCED
    - EARLY EXFOLIATION OF PRIMARY TEETH    HYPOPHOSPHOTASIA - LACK OF SERUM ALKALINE PHOSPHATASE - LITTLE CEMENTUM PRODUCED - EARLY EXFOLIATION OF PRIMARY TEETH
  57. 57—MELKERSSON ROSENTHAL SYNDROME
    - OROFACIAL GRANULOMATOSIS
    - FACIAL AND LIP SWELLING
    - FISSURED TONGUE    MELKERSSON ROSENTHAL SYNDROME - OROFACIAL GRANULOMATOSIS - FACIAL AND LIP SWELLING - FISSURED TONGUE
  58. 58—MULTIPLE ENDOCRINE NEOPLASIA 2B (MEN 2B)
    - MARFANOID BODY
    - FULL LIPS
    ABRAHAM LINCOLN
    - MUCOSAL NEUROMAS (LIP, TONGUE)
    -MEDULLARY THYROID CANCER    MULTIPLE ENDOCRINE NEOPLASIA 2B (MEN 2B) - MARFANOID BODY - FULL LIPS ABRAHAM LINCOLN - MUCOSAL NEUROMAS (LIP, TONGUE) -MEDULLARY THYROID...
  59. 59—BECKWITH-WIEDEMANN SYNDROME
    - MACROGLOSSIA
    - MICROCEPHALY
    - OMPHALOCELE - UNBILICAL HERNIA
    - RENAL ANOMALIES
    - NEOPLASMS (NEPHROBLASTOMAS)    BECKWITH-WIEDEMANN SYNDROME - MACROGLOSSIA - MICROCEPHALY - OMPHALOCELE - UNBILICAL HERNIA - RENAL ANOMALIES - NEOPLASMS (NEPHROBLASTOMAS)
  60. 60—STURGE WEBBER
    - PORT WINE STAIN - CAPILLARY VASCULAR MALFORMATION
    - OVERGROWTH OF BONY MAXILLA
    - GLAUCOMA --> BLINDNESS    STURGE WEBBER - PORT WINE STAIN - CAPILLARY VASCULAR MALFORMATION - OVERGROWTH OF BONY MAXILLA - GLAUCOMA --> BLINDNESS
  61. 61AMELOGENESIS IMPERFECTA TYPE IHYPOPLASTIC
    - POOR HISTODIFFERENTIATION
    - DEFECTIVE FORMATION OF ENAMEL MATRIX
    - INSUFFICIENT ENAMEL QUANTITY
    - UNDERSIZED CROWNS (OPEN BITE)
    - PITTED, YELLOW TO BROWN
    - X-RAY: THIN ENAMEL
  62. 62AI TYPE IIHYPOMATURATION
    - DEFECT IN MATURATION OF ENAMEL CRYSTAL
    - MOTTLED, WHITE, YELLOW-BROWN, SNOW CAPS
    - SOFT ENAMEL CHIPS
    - XRAY: ENAMEL RADIODENSE LIKE DENTIN
  63. 63AI TYPE IIIHYPOCALCIFIED
    - ADEQUATE ENAMEL MATRIX BUT MINIMAL MINERALIZATION
    - ANT OPEN BITE
    - DELAYED ERUPTION
    - SOFT ENAMEL, YELLOW TO DARK BROWN
    - CALCULUS
    - SENSITIVE TEETH
    - X-RAY: RADIODENSITY OF ENAMEL = DENTIN
  64. 64AI TYPE IVCOMBINED: HYPOPLASTIC + HYPOMATURATION + TAURODONTISM
    - CLOUDY WHITE - YELLOW/BROWN
    - NORMAL THICKNESS, MOTTLED SURFACE
  65. 65DENTINOGENESIS IMPERFECTA TYPE I- OCCURS WITH OSTEOGENESIS IMPERFECTA
    - SEVERITY: PRIMARY>PERM
    - BULBOUS CROWNS
    - SHORT THIN ROOTS
    - OBLITERATED ROOT CANALS B/C EXCESS DENTIN
    - RAPID ATTRITION
    - CLASS III - POST XBITE AND OPENBITE
    - AMBER TRANSLUCENCE
  66. 66OSTEOGENESIS IMPERFECTA- DEFECTIVE COLLAGEN
    - BOWING OF LEGS FRACTURES
    - BLUE SCLERA
    - IMPAIRED HEARING
    - MACROCEPHALY
    -TYPE II: PERINATALLY LETHAL
    TYPE III: PROGRESSIVE DEFORMING
  67. 67DENTINOGENESIS IMPERFECTA TYPE II- HEREDITARY OPALESCENT DENTIN
    - DEFECT OF PREDENTIN MATRIX
    - SAME CHARACTERISTICS AS TYPE I
    - AMBER BROWN TO BLUE GREY
    - SEVERE WEAR
    - BULBOUS CROWN
    - SHORT ROOTS
    - PCO, ECTOPIC ERUPTION
    - OVERLAPS FEATURES OF DD TYPE I
    TX: BLEACHING, COMP VENEERS, CROWNS, IMPLANT
  68. 68—DENTIN DYSPLASIA TYPE I
    Radicular Type
    - "ROOT-LESS"
    - DEFECT IN ROOT SHEATH
    - NORMAL CROWN
    - SHORT BLUNTED OR NO ROOT
    - PCO (PRIMARY)
    - CRESENT SHAPED CHAMBER (PERM)
    - PARs    DENTIN DYSPLASIA TYPE I Radicular Type - "ROOT-LESS" - DEFECT IN ROOT SHEATH - NORMAL CROWN - SHORT BLUNTED OR NO ROOT - PCO (PRIMARY) - ...
  69. 69—DENTIN DYSPLASIA TYPE II
    - Coronal type
    - PRIMARY LOOKS LIKE DI (AMBER COLORED, BULBOUS)
    - PERM: NORMAL CROWN, THISTLE TUBE OR FLAME SHAPED PULP, PULP STONES
    - BOTH HAVE NORMAL ROOTS LENGTH
    - No PARs    DENTIN DYSPLASIA TYPE II - Coronal type - PRIMARY LOOKS LIKE DI (AMBER COLORED, BULBOUS) - PERM: NORMAL CROWN, THISTLE TUBE OR FLAME SHAP...
  70. 70DI TYPE III- PRIMARY AND PERM
    - AMBER-BROWN
    - SEVERE, RAPID WEAR
    - SPONTANEOUS ABSCESS B/C LARGE PULP AND THIN DENTIN
    - SHELL TEETH
    - BELL SHAPED CROWNS
  71. 71REGIONAL ODONTOPLASIA- GHOST TEETH
    - ARREST IN TOOTH DEVELOPMENT
    - SHELL ENEMAL
    - LARGE PULP
    - LITTLE DENTIN
    - 80% INVOVLE CENTRALS
    - FAILURE OF TEETH TO ERUPT
  72. 72SYNDROMES WITH CLEFT PALATE- PIERRE ROBIN SEQUENCE
    - CLEIDOCRANIAL DYSPLASIA
    - DOWN SYNDROME
    - TRECHER COLLINS
    - APERT
    - OROFACIAL DIGITAL
    - VAN DER WOUDE
  73. 73SYNDROMES WITH MACROGLOSSIA- BECKWITH-WIEDEMANN
    - DOWN
    - MPS
    - NEUROFIBROMATOSIS
    - MEN 2B
  74. 74SYNDROMES WITH HYPERDONTIA- CLEIDOCRANIAL DYSPLASIA
    - GARDENER
    - APERT
    - CROUZON
    - DOWN
    - STURGE WEBBER
    - OROFACIAL DIGITAL
    - HALLERMAN STREIFF
    - CLP
  75. 75SYNDROMES WITH HYPODONTIA- ECTODERMAL DYSPLASIA
    - APERT
    - CROUZON
    - DOWN
    - HALLERMAN STREIFF
    - OROFACIAL DIGITAL
  76. 76TAURODONTISM- KLINEFELTER (XXY)
    - ECTODERMAL DYSPLASIA
    - DOWN SYNDROME
  77. 77ECTODERMAL DYSPLASIA- SPARSE HAIR, NAILS, SWEAT, TEETH
    - DENTURE ONLY 9 TEETH
    - HYPOPLASTIC ENAMEL AND MAXILLA
  78. 78VITAMIN D RESISTENT RICKETS- LARGE PULPS - EASILY ABSCESS
    - BOWED LEGS - SHORT
    - HYPOMINERALIZED DENTIN (NOT ENAMELL)
  79. 79—MELANOTIC NEUROECTODERMAL TUMOR OF INFANCY
    - DESTRUCTION OF ANTERIOR MAXILLA
    - FLOATING TOOTHBUDS
    - PIGMENTATION OF LESION
    - SMOOTH EXPANSILE LESION OF ALVEOLUS
    - SUNRAY
    - RARE AGRESSIVE TUMOR
    - URINE MARKER, INCREASED VANILLYLMANDELIC ACID    MELANOTIC NEUROECTODERMAL TUMOR OF INFANCY - DESTRUCTION OF ANTERIOR MAXILLA - FLOATING TOOTHBUDS - PIGMENTATION OF LESION - SMOOTH EXPAN...
  80. 80SYNDROMES WITH NATAL TEETHHALLERMAN STRIEFF AND ELLIS VAN CREVALD
  81. 81CHARGE SYNDROMENEWBORNS WITH CONGENITAL FEATURES
    - C = COLOMBOMA OF EYE
    - H = HEART DEFECTS
    - A = ATRESIA OF CHOANAE
    - R = RETARDATION OF GROWTH AND DEV.
    - G = GENITAL AND URINARY ABNORMALITIES
    - E = EAR ABNORMALITIES AND DEAFNESS
  82. 82NOONAN SYNDROME- Congenital Heart Defects and Bleeding disorders
    - Short
    - Webbed Neck
    - Micrognathia
    - Learning Disability
    - Deep Filtrum
  83. 83STICKLER SYNDROME- MIDFACE DEFICIENCY
    - CP NO CL
    - BIFID UVULA
    - HIGH PALATAL ARCH
  84. 84SYNDROMES WITH ATLANTO-AXIAL INSTABILITY- C1/C2
    - DOWN
    - ACHONDROPLASIA
  85. 85SYNDROMES WITH BIFID UVULA- STICKLER
    - SUBMUCOUS CLEFT
  86. 86BIFID TONGUE- ORO-FACIAL-DIGITAL
  87. 87GORLIN SYNDROME- NEVOID BASAL CELL CARCINOMA
    - OKC
    - SKELETAL ANOMALIES
  88. 88GORLIN CYST- CALCIFYING ODONTOGENIC CYST
  89. 89—DENTINOGENESIS IMPERFECTA
    - Opalescent
    - Enamel breaks off of thin dentin easily
    - Type 1: OI (mostly primary)
    Type 2: Primary and perm
    Both: Obliterated Pulp Space
    Both: Bulbous crown, short roots    DENTINOGENESIS IMPERFECTA - Opalescent - Enamel breaks off of thin dentin easily - Type 1: OI (mostly primary) Type 2: Primary and perm B...
  90. 90—Beckwith-Wiedemann Syndrome
    - Macroglossia
    - Ear Creases
    - Omphalocele or umbilical hernia
    - Severe Hypoglycemia
    - High Cancer Risk (Nephroblastoma)
    - Microcephaly    Beckwith-Wiedemann Syndrome - Macroglossia - Ear Creases - Omphalocele or umbilical hernia - Severe Hypoglycemia - High Cancer Risk (Neph...
  91. 91Lesch-Nyhan Syndrome- Spastic Cerebral Palsy
    - Bizarre self-mutilating behavior
    - Mental disability
  92. 92Peutz-Jeghers Syndrome- Stigmata - mucocutaneous pigmentation (lip freckles) and intestinal polyps
    - Anemia, rectal bleeding
    - Increased risk of developing colon cancer
  93. 93Gorlin Syndrome- Multiple Odontogenic Keratocysts (OKCs), Cleft Lip and Palate
    - Skin: Multiple Nevoid Basal Cell Carinoma
    - Skeletal: Rib anomalies, Vertebral deformities, polydactyly
    - CNS: Calcified falx cerebri, brain tumors
  94. 94Syndromes Associated with Pierre Robin Sequence- Velocariofacial Syndrome
    - Treacher Collins
    - Stickler
    - CHARGE
  95. 95Velocardiofacial Syndrome (DiGeorge Syndrome)- Long bulbous nose, low set malformed ears, long slender fingers
    - Cardiac Abnormality
    - Cleft Palate common - Immune def common
    - Hypoparathyroidism -> hypocalcemia -> Take Vitamin D and Calcium
  96. 96Williams Syndrome- Elf-like
    - Cardiac problems
  97. 97Prader Willi Syndrome- Most common form of obesity caused by genetic syndrome
    - Infantile Central Hypotonia
    -
  98. 98Womanly manKlinefelter
    XXY
  99. 99Papillon-Lefevre Syndrome- Severe destruction of periodontium results in loss of most primary teeth by age of 4 and most permanent teeth by age 14
    - hyperkeratosis of palms and soles of feet
  100. 100Chediak Higashi Syndrome- Partial Albanism - pale colored hair, eyes and skin
    - Rare dz of immune and nervous system
    - Recurrent pyogenic infection
  101. 101Kawasaki Dz- Strawberry Tongue
    - Coronary artery aneurysm
  102. 102Fragile X- Most widespread single gene cause of autism and inherited mental retardation
    - Large ears and long face
  103. 103What causes Cleft lip without palate? What causes Cleft Palate?- Failure of fusion of maxillary and medial nasal process
  104. 104What causes cleft lip without cleft palate? Whats causes cleft palate?- Cleft Lip: Failure of fusion of maxillary and medial nasal processes
    - Cleft Palate: Failure of fusion of lateral palatine processes
  105. 105Stages of Repair for CL/CP0-3 months: pre-surgery orthopedics to narrow cleft (Nasoalveolar molding, lip taping), possible lip adhesion surgery
    3-6 months: Cheiloplasty
    10-18 months: Palatoplasty
    2-5 years: Lip and nose revision (maybe secondary palate surgery for speech)
    6-11 years: Alveolar bone graft surgery
    12-18 years: Lip revision, jaw surgery, rhinoplasty
    Adult: Final surgeries

Information

Description
Flashcards on SYNDROMES, created by Khu gh on 12/09/2021.
Created by
Khu gh
Views
15
Rating

More on Developmental Abnormalities of Teeth and Face

Feedback

What is it about?

What do you think of the new look?

How do you like it?