Langer-Giedion Syndrome: a Rare Case Report

Langer-Giedion syndrome is a very uncommon autosomal dominant genetic disorder caused by the deletion of chromosomal material. It is characterized by multiple bony exostosis, short stature, mental retardation, and typical facial features. The characteristic appearance of individuals includes sparse...

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Detalles Bibliográficos
Autores principales: Katge, Farhin Ali, Rusawat, Bhavesh Dahyabhai, Shivasharan, Pooja Ravindra, Patil, Devendra Pandurang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University of Medical Sciences 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006835/
https://www.ncbi.nlm.nih.gov/pubmed/27602401

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006835/
https://www.ncbi.nlm.nih.gov/pubmed/27602401

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