Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review

Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review

<h3>Background</h3><p dir="ltr">Möbius (Moebius) and Poland’s syndromes are two rare congenital syndromes characterized by non-progressive bilateral (and often asymmetric) dysfunction of the 6th and 7th cranial nerves and hypoplasia of the pectoral muscles associated with...

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Bibliographic Details
Main Author: Graeme E. Glass (17545758) (author)
Other Authors: Shiyas Mohammedali (15220171) (author), Bran Sivakumar (6819863) (author), Mitchell A. Stotland (15220174) (author), Faisal Abdulkader (15220177) (author), Debra O. Prosser (15220180) (author), Donald R. Love (14151258) (author)
Published: 2022
Subjects:
Biomedical and clinical sciences
Clinical sciences
Neurosciences
Möbius
Moebius
Poland syndrome
Symbrachydactyly
Pectoralis hypoplasia
Case report
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