Sifrim-Hitz-Weiss syndrome

A rare multiple congenital anomalies/dysmorphic syndrome due to CHD4 gene mutations. It is characterized by developmental delay, speech delay and variable degree of intellectual disability (mostly mid-to-moderate but some patients may also have normal intelligence). Even though clinical manifestations are significantly variable among patients, most patients manifest dysmorphic facial features (could sometimes include macrocephaly), congenital heart defects, hypotonia and opthalmologic abnormalities. Other clinical features may include brain structure anomalies, skeletal anomalies, hearing impairment and hypogonadism (only in males).

Also known as: CHD4-related neurodevelopmental disorder, SIHIWES, Sifrim-Hitz-Weiss syndrome, Sifrim-Hitz-Weiss syndrome; SIHIWES, Sifrim-Hitz-Weiss multiple congenital anomalies-intellectual disability syndrome, Sifrim-Hitz-Weiss multiple congenital anomalies-mental retardation syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Sifrim-Hitz-Weiss syndrome itself.