ReviewThe Pan African medical journal2020
Aplasia cutis congenita: a report of two cases from National Hospital Abuja, Nigeria and review of the literature.
Review in The Pan African medical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 31 citations in OpenAlex.
- Aplasia Cutis Congenita in Bart's Syndrome: A Case Report and Literature Review.Clinical case reports · 2026Article
- A Case Report of Postoperative Cystic Hydrocephalus Following Duroplasty and Scalp Reconstruction in Neonatal With Aplasia Cutis Congenita and Extensive Craniodural Defect.Case reports in surgery · 2026Article
- Surgical management of aplasia cutis congenita of the scalp and skull defect in a resource-limited setting: A case report.Surgical neurology international · 2026Article
- Case Report: A newFrontiers in medicine · 2026Article
- Pseudodidymosis aplasticosebacea: Binary phenomenon of congenital aplasia cutis congenita and nevus sebaceus.JAAD case reports · 2024Article
- Aplasia cutis congenita of extremities (group VII): case report from North-Western Nigeria.Sudanese journal of paediatrics · 2023Article
- Bart's syndrome associated with a disorder of sexual differentiation: An atypical presentation in a Cameroonian newborn.Clinical case reports · 2022Article
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Aplasia cutis congenita is a rare congenital abnormality first described in 1767 by cordon. It mostly appears as a solitary lesion involving various layers of the skin and sometimes the bone on the scalp, limbs or abdomen. Genetics, environmental and exogenous causes have been implicated as potential causes. Only about 500 cases have been reported globally as of 2013. Two cases of Aplasia Cutis Congenita (ACC) who presented with scalp and bone defects at birth are reported, one in a syndromic child delivered to a consanguineous family, with associated cardiac, skin and nail anomalies (likely Adams Oliver syndrome) and the other as an isolated scalp lesion. Both were large defects managed conservatively by a multidisciplinary team. The challenges of investigating and managing such complex scalp anomalies in sub-Saharan Africa are highlighted.
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Registered trials
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