Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review
Abstract Background 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 chest wall and upper limb anomalies res...
Main Authors: | Graeme E. Glass, Shiyas Mohammedali, Bran Sivakumar, Mitchell A. Stotland, Faisal Abdulkader, Debra O. Prosser, Donald R. Love |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2022-12-01
|
Series: | BMC Pediatrics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12887-022-03803-3 |
Similar Items
-
Moebius Syndrome Associated with Pectoral Muscle Hypoplasia: Case Report
by: Serkan Kılbaş, et al.
Published: (2010-12-01) -
Moebius Syndrome Associated with Pectoral Muscle Hypoplasia: Case Report
by: Serkan Kılbaş, et al.
Published: (2010-12-01) -
Mobius inversion in physics /
by: Chen, Nanxian, 1937-
Published: (c201) -
Autism and Möbius sequence: an exploratory study of children in northeastern Brazil
by: José Marcelino Bandim, et al.
Published: (2003-06-01) -
Eye Involvement in Möbius Syndrome and its Treatment
by: Tuğba Güngör Kızıloğlu, et al.
Published: (2011-12-01)