Top Smith-Magenis Syndrome Treatment Doctors in India
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040-68334455Frequently Asked Questions
Smith Magenis Syndrome (SMS) is a rare genetic condition caused by changes in chromosome 17, affecting development and certain daily functions.
Smith Magenis Syndrome is considered rare, with only a few thousand reported cases worldwide.
SMS can affect both males and females, usually identified in childhood due to developmental differences.
Most cases of SMS occur due to spontaneous genetic changes, but in rare instances, it can be passed from parent to child.
Yes, there are dedicated organisations, support groups and online communities that provide guidance and resources for families managing SMS.