Τρίτη 18 Οκτωβρίου 2016

Coffin siris syndrome: a rare clinical entity

2016-10-18T03-40-29Z
Source: International Journal of Contemporary Pediatrics
Rupali Jain, Sandip Gediya, Amzad Khan, Suresh Goyal, Lakhan Poswal.
Coffin-siris syndrome (CSS) is a rare, clinically heterogeneous disorder considered in the setting of prenatal onset of mild to moderate growth deficiency, facial dysmorphism, cognitive/developmental delay, and speech impairment, moderate to severe hypotonia, seizures and 5th finger/nail hypoplasia. The child had distinctive features of CSS like developmental delay, seizures, and coarse facial features, body hypertrichosis, scalp hypotrichosis and SNHL.


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