Gamuts

Congenital skull defect

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 Cause
Cerebrospinal fluid rhinorrhea
May Be Caused by
Aase syndrome
Acalvaria
Adams-Oliver syndrome
Aminopterin fetopathy
Aminopterin-fetopathy-like syndrome
Amniotic band syndrome
Bardet-Biedl syndrome
Cleidocranial dysostosis
Congenital fibromatosis
Congenital frontal bone defect with intact overlying scalp
Crane-Heise syndrome
Cranium bifidum occultum
Delleman syndrome
Dermal sinus
Ehlers-Danlos syndrome
Encephalocele
Epidermoid
Familial skull doughnut lesion
Fetal rubella infection
Frontal bone defect
Frontonasal dysplasia
Hallermann-Streiff syndrome
Hydrocephalus
Hydrops - ectopic calcification - moth-eaten skeletal dysplasia
Hyperparathyroidism
Hypochondrogenesis
Hypophosphatasia
Hypothyroidism
Lacunar skull
Lethal osteosclerotic skeletal dysplasia Astley-Kendall type
Menkes disease
Metaphyseal chondrodysplasia Jansen type
Neurofibromatosis
Noonan syndrome
Occipital foramina
Osteogenesis imperfecta
Otopalatodigital syndrome type 1
Pachydermoperiostosis
Parietal foramina
Parietal foramina-clavicular hypoplasia dysplasia
Parietal thinning
Progeria
Pyknodysostosis
Restrictive dermatopathy
Rickets
Rubinstein-Taybi syndrome
Schinzel phocomelia
Trisomy 13
Trisomy 18
Trisomy 21
Zellweger syndrome

Copyright © 2022, Charles E. Kahn, Jr., MD, MS
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