Acro-callous syndrome: A case report

A malformative syndrome of unknown prevalence, the diagnosis is based on morphological ultrasound and magnetic resonance imaging of the fetus. The transmission is genetic and autosomal recessive. Courtnes has established 4 diagnostic criteria to affirm the acrocal syndrome and to eliminate the amalg...

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Detalles Bibliográficos
Autores principales: Lamrissi, A., Madri, F.E., Charkaoui, M., Mourabbih, M., Jalal, M., Bouhya, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218811/
https://www.ncbi.nlm.nih.gov/pubmed/35738142
http://dx.doi.org/10.1016/j.ijscr.2022.107210
Descripción
Sumario:A malformative syndrome of unknown prevalence, the diagnosis is based on morphological ultrasound and magnetic resonance imaging of the fetus. The transmission is genetic and autosomal recessive. Courtnes has established 4 diagnostic criteria to affirm the acrocal syndrome and to eliminate the amalgam with other polymalformative syndrome.

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