Literature DB >> 862297

Hereditary aplasia cutis congenita and associated defects. Three instances in one family and a survey of reported cases.

B R McMurray, L W Martin, P St John Dignan, M H Fogelson.   

Abstract

Hereditary aplasia cutis congenita (ACC) is a rare, dominantly inherited syndrome of scalp aplasia associated with defects of the underlying skull and absent distal phalanges of the feet. The scalp lesions are generally benign, but the increased risk of bleeding or meningitis may require skin grafting.

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Year:  1977        PMID: 862297     DOI: 10.1177/000992287701600705

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  3 in total

Review 1.  Congenital scalp and skull defects with terminal transverse limb anomalies (Adams-Oliver syndrome): report of three additional cases.

Authors:  E Jaeggi; C Kind; R Morger
Journal:  Eur J Pediatr       Date:  1990-05       Impact factor: 3.183

Review 2.  Congenital frontal bone defect with intact overlying scalp.

Authors:  S Chakrabortty; S Oi; H Suzuki; I Izawa; M Yamaguchi; N Tamaki; S Matsumoto
Journal:  Childs Nerv Syst       Date:  1993-12       Impact factor: 1.475

3.  Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance.

Authors:  M Buttiëns; J P Fryns; P Jonckheere; K Brouckmans-Buttiëns; H Van den Berghe
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

  3 in total

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