Gynecological Endocrinology · 2019 · 14 citations · 21 references
MedicineEndocrinologyGynecologyHuman GeneticsInfertilityReproductive EndocrinologyCongenital Reproductive AnomaliesCongenital Uterine AnomaliesFemale InfertilityGenetic DisordersOvarian DisordersPelvic Ultrasound46, Xx Gonadal Dysgenesis46, Xy Gonadal DysgenesisAutosomal Recessive InheritanceDisorders Of Sexual DifferentiationMenstrual AmenorrheaOvarian DysgenesisPrimary AmenorrheaWhole-exome Sequencing Analysis
Perrault syndrome is a rare autosomal recessive disorder that affects both males and females. The syndrome causes deafness in males, however females display gonadal dysgenesis along with sensorineural hearing loss. Herein, we present a 27-year-old female patient who is deaf and mute along with primary amenorrhea. Hormonal assays revealed hypergonadotropic hypogonadism and the karyotype was 46 XX. Pelvic ultrasound described a hypoplastic uterus and streak ovaries. MRI of the spine showed degenerative discs and Tarlov cysts. Whole exome sequencing identified a LARS2 mutation and the patient was diagnosed with Perrault syndrome type four (PRLTS4).
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Mitochondrial Stress Engages E2F1 Apoptotic Signaling to Cause Deafness
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