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SYNDROMES

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

Karten in diesem Stapel (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

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Karteikarten am SYNDROMES, erstellt von Khu gh am 12/09/2021.
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