Aarskog-Scott Syndrome: Clinico-Radiological Illustration of a Rare Case
<p>Aarskog-Scott Syndrome is a rare syndrome and is estimated to occur in 1 in 1 million individuals in general population. It is transmitted in an X-linked recessive manner and occurs due to FGD1 gene mutation. It has facial, genital and digital hands symptoms, musculoskeletal anomalies and a...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Global Journal of Rare Diseases - Peertechz Publications,
2016-12-30.
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