Developmental Anomalies Flashcards
Lack of fusion between medial nasal process with lateral portion of maxillary process
Cleft lip
Cleft lip occurs in
6th and 7th week of embryonic development
Unilateral cleft lip mostly occurs on which side
Left
Cleft palate occurs during
8th to 10th week of development
Failure of fusion of palatal shelves of the maxillary process
Cleft palate
Cleft or bifid uvula
Cleft palate
Most common form of craniofacial malformations of head and neck
Cleft lip and palate
Maternal alcohol consumption, maternal cigarettes smoking, anti convulsant therapy, folic acid deficiency
Cleft lip and palate
Speech & swallowing problems, malocclusion, crown defects missing teeth or supernumerary teeth
Cleft lip and palate
Lack of fusion between mandibular and maxillary processes
Lateral facial cleft
Congenital invaginations bilateral symmetric fistulas on lower lip
Paramedian Lip pits
Lower lip pits+cleft lip and palate
Van der woude syndrome
Group of inherited diseases by aplasia or hypoplasia of ectodermal structures
Ectodermal dysplasia
Hypohidrotic form, X linked recessive inheritance
Ectodermal dysplasia
Smooth dry skin, thin blonder hair and eyebrows, no sweat glands, heat intolerance, midface hypoplasia, brittle nails, xerostomia, anodontia/oligodontia
Ectodermal dysplasia
Autosomal dominant disorder affects face, skull and clavicles
Cleidocranial dysplasia
Mutation in gene RUNX2
Cleidocranial dysplasia
Hypoplasia or aplasia of clavicles, hyper mobility of shoulders, defective ossification of the skull, short skull broad based nose and ocular hypertelorism
Cleidocranial dysplasia
Over retention of deciduous teeth, failure of eruption of permanent teeth, supernumerary teeth, dentigerous cyst
Cleidocranial dysplasia
Cleft palate, micrognathia, hypoplasia, retrognathia of mandible, glossoptosis, airway obstruction
Pierre Robin syndrome
Autosomal condition malformation of skull
Apert syndrome/ Acrocephalosyndactyly
Craniosynostosis, Acrobrachycephaly, tower skull, hypertelorism, class III occlusion, retruded middle third
Apert syndrome
Bifid uvula, cleft palate, severe crowding, ant openbite, ant and post crossbite, shovel shaped incisors, delayed eruption, syndactyly
Apert syndrome
Brachycephaly, shallow orbits, ocular proptosis, hypertelorism, increased intra cranial pressure
Crouzon Syndrome (Craniofacial Dysostosis)