Article
A new patient with LACHT syndrome (Mardini-Nyhan association).
American journal of medical genetics. Part A - 1 Feb 2015
Atik Tahir, Torun Huseyin Ozan, Cogulu Ozgur, Ozkinay Ferda
Abstract excerpt
LACHT syndrome, Lung Agenesis, Congenital Heart defects, and Thumb anomalies, (Mardini-Nyhan Association OMIM #601612) is a rare condition characterized by unilateral or bilateral lung agenesis, complex cardiac defects, especially anomalous pulmonary venous return, and thumb anomalies. Based on previous cases, its inheritance pattern seems to be autosomal recessive. In 1985, the syndrome was firstly described by...
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