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ENPerrault Syndrome 3 (PRLTS3)
Alias:
Prlts3
Deafness, Autosomal Recessive 81, Formerly
Perrault Syndrome, Type 3
Dfnb81, Formerly
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Perrault Syndrome 3, also known as prlts3, is related to perrault syndrome and premature menopause. An important gene associated with Perrault Syndrome 3 is CLPP (Caseinolytic Mitochondrial Matrix Peptidase Proteolytic Subunit). Affiliated tissues include uterus and ovary, and related phenotypes are sensorineural hearing impairment and elevated circulating follicle stimulating hormone level
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MALACARDS
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