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Acro-callous syndrome: A case report. | LitMetric

Acro-callous syndrome: A case report.

Int J Surg Case Rep

Maternity Service, Mother and Child Hospital Abderrahim Harouchi, University Hospital IBN ROCHD of Casablanca, Morocco; Gynecology Obstetric Department, Faculty of Medicine and Pharmacy of Casablanca, Hassan 2 University of Casablanca, Morocco; Biology and Health Laboratory (LBS), Hassan 2 University of Casablanca, Morocco.

Published: July 2022

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218811PMC
http://dx.doi.org/10.1016/j.ijscr.2022.107210DOI Listing

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