Acro-callous syndrome: A case report

Autor: A. Lamrissi, F.E. Madri, M. Charkaoui, M. Mourabbih, M. Jalal, S. Bouhya
Rok vydání: 2022
Předmět:
Zdroj: International Journal of Surgery Case Reports. 96:107210
ISSN: 2210-2612
DOI: 10.1016/j.ijscr.2022.107210
Popis: 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.
Databáze: OpenAIRE