Cassia Stocco dos Santos syndrome: Difference between revisions

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==Overview==
==Overview==
Cassia Stocco dos Santos syndrome is autosomal recessive dieases with the prevalence rate of <1 / 1 000 000 and age of onset is infancy and neonates with characteristic features of  anophthalmia, megalocornea, cardiopathy, skeletal anomalies.
Cassia Stocco dos Santos syndrome is autosomal recessive disease with characteristic features of anophthalmia, megalocornea, cardiopathy and skeletal anomalies with the age of onset of infancy and neonates and the prevalence rate of <1 / 1 000 000.

Revision as of 15:21, 21 December 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Jyostna Chouturi, M.B.B.S [2]

Overview

Cassia Stocco dos Santos syndrome is autosomal recessive disease with characteristic features of anophthalmia, megalocornea, cardiopathy and skeletal anomalies with the age of onset of infancy and neonates and the prevalence rate of <1 / 1 000 000.