Smith-Lemli-Opitz syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by distinctive facial features ...
Smith-Lemli-Opitz syndrome (SLOS) is a multiple congenital anomalies (MCA)/mental retardation (MR) syndrome caused by a defect in cholesterol synthesis.
It is possible that the main title of the report Smith Lemli Opitz Syndrome is not the name you expected. Please check the synonyms listing to find the ...
SLOS phenotype and symptoms. SLOS can present itself differently in different cases, depending on the severity of the mutation and other factors.
Families and supporters of individuals with Smith-Lemli-Opitz Syndrome are encouraged to register NOW for the SLO Family Medical Conference, ... Smith-Lemli-Opitz ...
What is Smith-Lemli-Opitz syndrome (SLOS)? SLOS is a metabolic disorder caused by a mutation in the DHCR7 (7-dehydrocholesterol reductase) gene on chromosome 11.
Smith-Lemli-Opitz syndrome is an autosomal recessively inherited disorder. A severe defect in cholesterol biosynthesis has been identified leading to abnormally low ...
Smith-Lemli-Opitz Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
What is Smith-Lemli-Opitz Syndrome? Smith-Lemli-Opitz syndrome, or SLO syndrome, is an inherited disorder in which the body's ability to make cholesterol is impaired ...
General Discussion. Smith-Lemli-Opitz syndrome (SLOS) is a variable genetic disorder that is characterized by slow growth before and after birth, small head ...