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EN6q16 Microdeletion Syndrome
Alias:
Prader-Willi-Like Syndrome Due to Microdeletion 6q16
Monosomy 6q16
Del(6)(q16)
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6q16 Microdeletion Syndrome, is also known as prader-willi-like syndrome due to microdeletion 6q16. An important gene associated with 6q16 Microdeletion Syndrome is SIM1 (SIM BHLH Transcription Factor 1). Affiliated tissues include eye, and related phenotypes are global developmental delay and delayed speech and language development
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MALACARDS
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