Smith-Lemli-Opitz syndrome (SLOS) is a rare genetic condition affecting multiple body systems. Signs and symptoms may include characteristic facial features, small head size, growth and developmental delays, and intellectual and behavioral problems.

2021年11月17日 · Smith-Lemli-Opitz syndrome (SLOS) is a genetic condition that affects many parts of the body. It is an autosomal recessive genetic condition caused by changes in the DHCR7 gene. Problems associated with SLOS are usually noticeable before or …

The signs and symptoms of Smith-Lemli-Opitz syndrome vary widely. Mildly affected individuals may have only minor physical abnormalities with learning and behavioral problems. Severe cases can be life-threatening and involve profound intellectual …

Smith-Lemli-Opitz syndrome (SLOS) is a rare genetic condition affecting multiple body systems. Signs and symptoms may include characteristic facial features, small head size, growth and developmental delays, and intellectual and behavioral problems.

1998年11月13日 · Smith-Lemli-Opitz syndrome (SLOS) is a congenital multiple-anomaly / cognitive impairment syndrome caused by an abnormality in cholesterol metabolism resulting from deficiency of the enzyme 7-dehydrocholesterol (7-DHC) reductase.

What are the symptoms of Smith-Lemli-Opitz syndrome? Symptoms include intellectual disability, distinctive facial features, and abnormalities in the limbs and genitalia. The severity varies among individuals.

What are the main symptoms of Smith-Lemli-Opitz syndrome? Symptoms may vary from mild to moderate, but the main symptoms of Smith-Lemli-Opitz syndrome are behavioral and learning problems. Most individuals with the syndrome receive a separate diagnosis of autism or display autistic tendencies.

2024年1月11日 · Smith-Lemli-Opitz syndrome (SLOS) is a rare inherited condition characterized by a defect in cholesterol synthesis, resulting in low plasma cholesterol levels and raised levels of precursor 7-dehydrocholesterol (7-DHC).

2022年5月2日 · Smith-Lemli-Opitz syndrome (SLOS) is a rare genetic condition affecting multiple body systems. Signs and symptoms may include characteristic facial features, small head size, growth and developmental delays, and intellectual and behavioral problems.

2021年7月6日 · What are the symptoms of Smith-Lemli-Opitz Syndrome? Slow growth, a small head, intellectual disability, heart defects, extra fingers and toes (polydactyly), second and third toes joined together (syndactyly), cleft palate, underdeveloped external genitalia in boys are typical features.