Fraser Syndrome - a Case Report and Review of Literature

Fraser syndrome is a rare autosomal recessive genetic disorder characterized by major features such as cryptophthalmos, syndactyly, malformations of the larynx and genitourinary tract, craniofacial dysmorphism, orofacial clefting, mental retardation and musculoskeletal anomalies. In total, about 150...

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Guardat en:
Dades bibliogràfiques
Publicat a:Maedica (Bucur)
Autors principals: Dumitru, Adrian, Costache, Mariana, Lazaroiu, Anca Mihaela, Simion, George, Secara, Diana, Cirstoiu, Monica, Emanoil, Alina, Georgescu, Tiberiu Augustin, Sajin, Maria
Format: Artigo
Idioma:Inglês
Publicat: Tarus Media 2016
Matèries:
Case Reports
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5394498/
https://ncbi.nlm.nih.gov/pubmed/28465758
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