Thanatophoric dysplasia

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Abstract

Thanatophoric Dysplasia (TD) is a severe skeletal dysplasia that is lethal in the neonatal period. There are two defined TD subtypes which have been classified clinically. The incidence is approximately 1/20,000 to 1/50,000. Type I TD being more frequent than Type II. Most individuals with TD die within the first few hours.This condition has characteristic sonographic features detected antenatally by midgestation, although distinction from other short-limbed dysplasia syndromes may be difficult. We report a case of type I TD with typical clinicoradiological features who succumbed within one hour of life.

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APA

Badal, S., Shuvendu, R., & Daljit, S. (2015). Thanatophoric dysplasia. Journal of Nepal Paediatric Society, 35(3), 304–306. https://doi.org/10.3126/jnps.v35i3.11946

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