Smith Lemli Opitz Syndrome Genetic Disorders Conditions and Diseases

Smith-Lemli-Opitz syndrome is a hereditary developmental disorder. It is characterized by nostrils that tilt forward (anteverted nares), drooping eyelids, webbing between the second and third toes, male genital abnormalities, mental retardation, and small stature.

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• NORD: Smith Lemli Opitz Syndrome - Offers a brief description, the synonyms and further genetic disorders resources.
• Emergency Medicine - A article about Smith-Lemli-Opitz syndrome, a multiple genetic disorders congenital anomalies/mental retardation syndrome caused by a defect genetic disorders in cholesterol synthesis.
• Smith-Lemli-Opitz/RSH Foundation - The Smith-Lemli-Opitz/RSH Foundation was created in 1988 to give a conditions and diseases group of 37 families with SLO/RSH children a network to conditions and diseases exchange experiences and information about SLO/RSH. Since then, the group conditions and diseases has grown to more than 200 families in the United conditions and diseases States a

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