Article
Diagnosis of Achondroplasia at Birth: A Case Report.
JNMA; journal of the Nepal Medical Association - 1 Feb 2020
Bhusal Suzit, Gautam Uttara, Phuyal Rajan, Choudhary Robin, Manandhar Sunil Raja, Niroula Aliska
Abstract excerpt
Autosomal dominant mutations in fibroblast growth factor receptor 3 cause achondroplasia, the most common form of dwarfism in humans. Achondroplasia is a genetic disorder causing rhizomelic shortening of limbs. Head is often large with prominent forehead causing vaginal delivery difficult. A twenty-one years old multipara mother gave birth to a baby with achondroplasia via spontaneous vaginal delivery with...
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