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
Beaten metal radio appearance
Crouzon syndrome
26
Calcified stylohyoid ligament
Eagle syndrome
27
Developmental anomaly of first and second branchial arch structures, hypoplastic zygoma, narrow face, downward slanting palpebral fissures, ear defects
Treacher collin syndrome
28
Mandibular hypoplasia, retruded chin, cleft palate, severe midface deficiency, malocclusion, condyle and coronoid process flattened and aplastic
Treacher Collins syndrome
29
Trisomy 21, delayed mental and physical development, congenital heart disease, epilepsy
Down syndrome
30
Short, stocky build, broad flat face, ocular hypotelorism, upward slanting palpabral fissures, flattened nasal bridge
Down syndrome
31
Macroglossia, mouth breathing, openbite, increased perio disease, mandibular prognathism
Down syndrome
32
Multinodular enlarged tongue, crenated lateral border to the tongue
Macroglossia
33
Localized lingual gingival recession, restricted tongue movement, speech swallowing problems
Ankyloglossia
34
Fissured tongue seen in
Geographic tongue, Down syndrome, Melkersson-Rosenthal syndrome
35
Excessive growth on one of the condyles, facial asymmetry, prognathism, cross bite, open bite
Condylar Hyperplasia
36
Mandible deviates to the unaffected site
Condylar hyperplasia
37
Small mandible, class II malocclusion, underdevelopment of mandible, depression of face to affected side. Mand midline shifted to affected side when mouth is open
Condylar Hypoplasia
38
Asymmetric overgrowth of one or more body parts
Hemihyperplasia
39
Group of disorders affecting body movement and muscle coordination
Cerebral palsy
40
Spastic paralysis or impairment of control or coordination, mental retardation, seizures, disorders of vision and communication
Cerebral palsy