A New Case of Neu–Laxova Syndrome: Infant with Facial Dysmorphism, Arthrogryposis, Ichthyosis, and Microcephalia

Neu–Laxova syndrome (NLS) is an autosomal recessive disorder characterized by central nervous system anomalies, facial dysmorphic features, anomalies of limb and genitalia, intrauterine growth retardation, skin disorders, and other congenital abnormalities. In this article, we present a newborn infa...

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Detalles Bibliográficos
Autores principales: Barekatain, Behzad, Sadeghnia, Alireza, Rouhani, Elham, Soofi, Ghazaleh Jamalipoor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952546/
https://www.ncbi.nlm.nih.gov/pubmed/29862217
http://dx.doi.org/10.4103/abr.abr_143_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952546/
https://www.ncbi.nlm.nih.gov/pubmed/29862217
http://dx.doi.org/10.4103/abr.abr_143_17

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