Gamuts

Skin aplasia

Aplasia cutis congenita is a rare disorder characterized by congenital absence of skin. Frieden classified ACC in 1986 into 9 groups on the basis of location of the lesions and associated congenital anomalies. [Source: Wikipedia ]

May Be Caused by
Acrogeria
Aplasia cutis congenita
Ataxia-telangiectasia
Barber-Say syndrome
Chromosome 4p- syndrome
Congenital scalp defect and postaxial polydactyly
CREST syndrome
Delleman syndrome
Dysosteosclerosis
Ehlers-Danlos
Flynn-Aird syndrome
Focal scleroderma
Goltz syndrome
Hallermann-Streiff syndrome
Incontinentia pigmenti
Kindler syndrome
Knobloch syndrome
Mandibuloacral dysplasia
MIDAS syndrome
Occipital scalp defect and valvular pulmonary stenosis
Oculo-auriculo-vertebral spectrum
Oculoectodermal syndrome
Progeria
Rothmund-Thomson syndrome
Sakati syndrome
Scalp-ear-nipple syndrome
Scleroderma
Setleis syndrome
Trichorhinophalangeal dysplasia type 3
Trisomy 13
Weber-Christian syndrome
Werner syndrome

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