Searching for Aarskog Scott Syndrome Support information? Find all needed info by using official links provided below.
https://ghr.nlm.nih.gov/condition/aarskog-scott-syndrome
Oct 15, 2019 · Aarskog-Scott syndrome is a genetic disorder that affects the development of many parts of the body. This condition mainly affects males, although females may have mild features of the syndrome. People with Aarskog-Scott syndrome often have distinctive facial features, such as widely spaced eyes (hypertelorism), a small nose, a long area between the nose and mouth (philtrum), and a …
https://medlineplus.gov/ency/article/001654.htm
Aarskog syndrome is a genetic disorder that is linked to the X chromosome. It affects mainly males, but females may have a milder form. The condition is caused by changes (mutations) in a gene called "faciogenital dysplasia" (FGD1).
https://contact.org.uk/advice-and-support/medical-information/conditions/a/aarskog-syndrome/
The Aarskog Foundation UK aims to provide support to all those affected by Aarskog Syndrome, their friends, families and carers. They provide information, raise awareness of the condition and aim to bring families together.They also have different Facebook Groups to support families and professionals. Group details added March 2017.
https://www.aarskogsyndromefoundation.co.uk/
The Aarskog Foundation. We are the worlds largest international parent led, patient Charity for the X-linked Rare Disease Aarskog Syndrome. The lives of around 0.4 per million people across the world are living with this Rare Disease, which progresses into a serious life long condition of …
https://rarediseases.info.nih.gov/diseases/4775/aarskog-syndrome
76 rows · Sep 07, 2011 · Aarskog syndrome is an inherited disease that affects a person's height, …
https://globalgenes.org/disease/aarskog-scott-syndrome/
Aarskog syndrome is a genetic condition that affects a person’s physical and mental development. Features of this condition include unique facial features, such as wide-set eyes (hypertelorism), a small nose, and a widow’s peak, as well as short fingers (brachydactyly) and extra skin between the fingers (syndactyly). Other features of this syndrome can include heart
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155891/
Dec 05, 2012 · Aarskog-Scott syndrome (ASS), also named faciogenital dysplasia, is a rare syndrome that mainly affects the musculoskeletal system of male individuals, related with X-linked and mutations in FGD1 (Online Mendelian Inheritance in Man # 305400). It has facial, genital and digital hands symptoms.
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