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Aplasia Cutis Congenita on the Scalp

Year: 2025

Type: article

Abstract: Aplasia cutis congenita is a rare condition characterized by localized absent skin at birth, often affecting the scalp. The exact pathogenesis is unclear, but it is likely related to disrupted prenatal skin development. Potential etiologies include genetic factors, trauma, intrauterine infections, teratogens, incomplete neural tube closure, and vascular compromise. We present a case of aplasia cutis congenita on the scalp potentially associated with maternal methimazole use.

Source: Journal of the ASEAN Federation of Endocrine Societies

DOI: 10.15605/jafes.040.01.11

Authors: Supasuta Wongdama, Chutintorn Sriphrapradang

Institutions: Mahidol University, Ramathibodi Hospital

Language: English

Topic: Genetic and rare skin diseases.

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: diamond

OpenAlex ID: W4409988009

FWCI:

Cites: 4

Cited by:

Related to: 10