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...

Descripción completa

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
_version_ 1784731975778566144
author Lamrissi, A.
Madri, F.E.
Charkaoui, M.
Mourabbih, M.
Jalal, M.
Bouhya, S.
author_facet Lamrissi, A.
Madri, F.E.
Charkaoui, M.
Mourabbih, M.
Jalal, M.
Bouhya, S.
author_sort Lamrissi, A.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-9218811
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-92188112022-06-24 Acro-callous syndrome: A case report Lamrissi, A. Madri, F.E. Charkaoui, M. Mourabbih, M. Jalal, M. Bouhya, S. Int J Surg Case Rep 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 amalgam with other polymalformative syndrome. Elsevier 2022-05-20 /pmc/articles/PMC9218811/ /pubmed/35738142 http://dx.doi.org/10.1016/j.ijscr.2022.107210 Text en © 2022 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Lamrissi, A.
Madri, F.E.
Charkaoui, M.
Mourabbih, M.
Jalal, M.
Bouhya, S.
Acro-callous syndrome: A case report
title Acro-callous syndrome: A case report
title_full Acro-callous syndrome: A case report
title_fullStr Acro-callous syndrome: A case report
title_full_unstemmed Acro-callous syndrome: A case report
title_short Acro-callous syndrome: A case report
title_sort acro-callous syndrome: a case report
topic Case Report
url 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
work_keys_str_mv AT lamrissia acrocalloussyndromeacasereport
AT madrife acrocalloussyndromeacasereport
AT charkaouim acrocalloussyndromeacasereport
AT mourabbihm acrocalloussyndromeacasereport
AT jalalm acrocalloussyndromeacasereport
AT bouhyas acrocalloussyndromeacasereport

Ejemplares similares