Find all needed information about Smith Lemli Opitz Syndrome Support Agencies. Below you can see links where you can find everything you want to know about Smith Lemli Opitz Syndrome Support Agencies.
https://www.smithlemliopitz.org/
Smith-Lemli-Opitz RSH Foundation is a non-profit organization dedicated to supporting families, individuals and professionals dealing with Smith-Lemli-Opitz syndrome. By providing a network of ongoing communication, funding related research, and raising awareness, we are com mitted to enhancing the quality of life of affected individuals ...
https://www.nicklauschildrens.org/conditions/opitz-syndrome
Smith-Lemli-Opitz syndrome is a genetic disorder that presents with slow growth before and after birth and multiple anomalies at birth. We use cookies to personalize content and ads, to provide social media features, and to analyze our traffic.
https://rarediseases.info.nih.gov/diseases/5683/smithlemliopitz-syndrome-type-1
158 rows · Smith-Lemli-Opitz syndrome is a developmental disorder characterized by distinctive …
https://www.diseaseinfosearch.org/disease/6648/support
The Smith-Lemli-Opitz/RSH Foundation is a non-profit organization dedicated to supporting families, individuals and professionals dealing with Smith-Lemli-Opitz syndrome. By providing a network of ongoing communication, funding related research, and raising awareness, we are committed to enhancing the quality of ...
https://www.verywellhealth.com/smith-lemli-opitz-syndrome-4772315
Smith Lemli Opitz syndrome is a congenital developmental disorder characterized by distinctive facial features, intellectual and learning disability, behavioral issues, and small head (microcephaly), among other manifestations.Alongside malformations of important organs like the kidneys, heart, genitals, and intestinal tract, children with this condition display characteristics of autism and ...
https://contact.org.uk/advice-and-support/medical-information/conditions/s/smith-lemli-opitz-syndrome/
Smith-Lemli-Opitz syndrome (SLOS) is a rare autosomal recessive disorder of cholesterol synthesis caused by mutations in 3β-hydroxysterol Δ7-reductase (DHCR7) gene. The estimated incidence of SLOS is between 1 in 20,000 to 1 in 40,000 live births, but may be higher.
https://www.smithlemliopitz.org/frequently-asked-questions/slos-overview/
SLOS Overview Smith-Lemli-Optiz syndrome, in layman’s terms, is the inability to correctly produce or synthesize cholesterol due to a low occurrence of the 7-DHC reductace enzyme. Cholesterol is an essential nutrient for every cell in a person’s body.
https://ghr.nlm.nih.gov/condition/smith-lemli-opitz-syndrome
Oct 29, 2019 · Smith-Lemli-Opitz syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by distinctive facial features, small head size (microcephaly), intellectual disability or learning problems, and behavioral problems.
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