Dubowitz syndrome is a rare autosomal recessive disorder characterized by micorcephaly, short stature, abnormal faces, and mild to severe mental retardation.
Important It is possible that the main title of the report Dubowitz Syndrome is not the name you expected. Please check the synonyms listing to find the alternate ...
Dubowitz syndrome is a rare genetic disorder characterized by microcephaly, growth retardation and a characteristic facial appearance (small, round, triangular shaped ...
What is Dubowitz syndrome? This is a development and genetic disorder that involves multiple inherited abnormalities including but not necessarily narrowed to:
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Dubowitz syndrome
Dubowitz Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Dubowitz syndrome is a very rare genetic and developmental disorder involving multiple congenital (inherited) anomalies including but not limited to: (1) growth ...
What is Dubowitz Syndrome? Adapted from the Online Mendelian Inheritance in Man/Johns Hopkins University. Dubowitz Syndrome is a rare syndrome found in approximately ...
223370 - DUBOWITZ SYNDROME ... NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic ...
Summary. Dubowitz syndrome (DS) is a rare multiple congenital syndrome characterized primarly by growth retardation, microcephaly, distinctive facial dysmorphism ...