Developmental Anomalies Flashcards

1
Q

Lack of fusion between medial nasal process with lateral portion of maxillary process

A

Cleft lip

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2
Q

Cleft lip occurs in

A

6th and 7th week of embryonic development

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3
Q

Unilateral cleft lip mostly occurs on which side

A

Left

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4
Q

Cleft palate occurs during

A

8th to 10th week of development

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5
Q

Failure of fusion of palatal shelves of the maxillary process

A

Cleft palate

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6
Q

Cleft or bifid uvula

A

Cleft palate

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7
Q

Most common form of craniofacial malformations of head and neck

A

Cleft lip and palate

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8
Q

Maternal alcohol consumption, maternal cigarettes smoking, anti convulsant therapy, folic acid deficiency

A

Cleft lip and palate

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9
Q

Speech & swallowing problems, malocclusion, crown defects missing teeth or supernumerary teeth

A

Cleft lip and palate

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10
Q

Lack of fusion between mandibular and maxillary processes

A

Lateral facial cleft

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11
Q

Congenital invaginations bilateral symmetric fistulas on lower lip

A

Paramedian Lip pits

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12
Q

Lower lip pits+cleft lip and palate

A

Van der woude syndrome

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13
Q

Group of inherited diseases by aplasia or hypoplasia of ectodermal structures

A

Ectodermal dysplasia

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14
Q

Hypohidrotic form, X linked recessive inheritance

A

Ectodermal dysplasia

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15
Q

Smooth dry skin, thin blonder hair and eyebrows, no sweat glands, heat intolerance, midface hypoplasia, brittle nails, xerostomia, anodontia/oligodontia

A

Ectodermal dysplasia

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16
Q

Autosomal dominant disorder affects face, skull and clavicles

A

Cleidocranial dysplasia

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17
Q

Mutation in gene RUNX2

A

Cleidocranial dysplasia

18
Q

Hypoplasia or aplasia of clavicles, hyper mobility of shoulders, defective ossification of the skull, short skull broad based nose and ocular hypertelorism

A

Cleidocranial dysplasia

19
Q

Over retention of deciduous teeth, failure of eruption of permanent teeth, supernumerary teeth, dentigerous cyst

A

Cleidocranial dysplasia

20
Q

Cleft palate, micrognathia, hypoplasia, retrognathia of mandible, glossoptosis, airway obstruction

A

Pierre Robin syndrome

21
Q

Autosomal condition malformation of skull

A

Apert syndrome/ Acrocephalosyndactyly

22
Q

Craniosynostosis, Acrobrachycephaly, tower skull, hypertelorism, class III occlusion, retruded middle third

A

Apert syndrome

23
Q

Bifid uvula, cleft palate, severe crowding, ant openbite, ant and post crossbite, shovel shaped incisors, delayed eruption, syndactyly

A

Apert syndrome

24
Q

Brachycephaly, shallow orbits, ocular proptosis, hypertelorism, increased intra cranial pressure

A

Crouzon Syndrome (Craniofacial Dysostosis)

25
Q

Beaten metal radio appearance

A

Crouzon syndrome

26
Q

Calcified stylohyoid ligament

A

Eagle syndrome

27
Q

Developmental anomaly of first and second branchial arch structures, hypoplastic zygoma, narrow face, downward slanting palpebral fissures, ear defects

A

Treacher collin syndrome

28
Q

Mandibular hypoplasia, retruded chin, cleft palate, severe midface deficiency, malocclusion, condyle and coronoid process flattened and aplastic

A

Treacher Collins syndrome

29
Q

Trisomy 21, delayed mental and physical development, congenital heart disease, epilepsy

A

Down syndrome

30
Q

Short, stocky build, broad flat face, ocular hypotelorism, upward slanting palpabral fissures, flattened nasal bridge

A

Down syndrome

31
Q

Macroglossia, mouth breathing, openbite, increased perio disease, mandibular prognathism

A

Down syndrome

32
Q

Multinodular enlarged tongue, crenated lateral border to the tongue

A

Macroglossia

33
Q

Localized lingual gingival recession, restricted tongue movement, speech swallowing problems

A

Ankyloglossia

34
Q

Fissured tongue seen in

A

Geographic tongue, Down syndrome, Melkersson-Rosenthal syndrome

35
Q

Excessive growth on one of the condyles, facial asymmetry, prognathism, cross bite, open bite

A

Condylar Hyperplasia

36
Q

Mandible deviates to the unaffected site

A

Condylar hyperplasia

37
Q

Small mandible, class II malocclusion, underdevelopment of mandible, depression of face to affected side. Mand midline shifted to affected side when mouth is open

A

Condylar Hypoplasia

38
Q

Asymmetric overgrowth of one or more body parts

A

Hemihyperplasia

39
Q

Group of disorders affecting body movement and muscle coordination

A

Cerebral palsy

40
Q

Spastic paralysis or impairment of control or coordination, mental retardation, seizures, disorders of vision and communication

A

Cerebral palsy