Open AccessA New Case of Neu–Laxova Syndrome: Infant with Facial Dysmorphism, Arthrogryposis, Ichthyosis, and Microcephalia
Author(s) -
Behzad Barekatain,
Alireza Sadeghnia,
Elham Rouhani,
Ghazaleh Jamalipoor Soofi
Publication year - 2018
Publication title -
advanced biomedical research
Language(s) - English
Resource type - Journals
ISSN - 2277-9175
DOI - 10.4103/abr.abr_143_17
Subject(s) - arthrogryposis , medicine , facial dysmorphism , ichthyosis , muscle contracture , dermatology , nose , facial muscles , pediatrics , anatomy , genetics , biology , gene , phenotype