Literature DB >> 31274036

Perrault syndrome with amenorrhea, infertility, Tarlov cyst, and degenerative disc.

Dania Al-Jaroudi1,2, Saed Enabi3, Malak Sameer AlThagafi4,5,6.   

Abstract

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).

Entities:  

Keywords:  Perrault syndrome; Primary amenorrhea; Tarlov cyst; bilateral ovarian dysgenesis; degenerative disc; hypo plastic uterus; primary infertility; sensorineural hearing loss

Mesh:

Substances:

Year:  2019        PMID: 31274036     DOI: 10.1080/09513590.2019.1637407

Source DB:  PubMed          Journal:  Gynecol Endocrinol        ISSN: 0951-3590            Impact factor:   2.260


  6 in total

1.  LARS2-Perrault syndrome: a new case report and literature review.

Authors:  Maria Teresa Carminho-Rodrigues; Phillipe Klee; Sacha Laurent; Michel Guipponi; Marc Abramowicz; Hélène Cao-van; Nils Guinand; Ariane Paoloni-Giacobino
Journal:  BMC Med Genet       Date:  2020-05-18       Impact factor: 2.103

2.  Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.

Authors:  Raffaella Rossetti; Silvia Moleri; Fabiana Guizzardi; Davide Gentilini; Laura Libera; Anna Marozzi; Costanzo Moretti; Francesco Brancati; Marco Bonomi; Luca Persani
Journal:  Front Endocrinol (Lausanne)       Date:  2021-11-04       Impact factor: 5.555

Review 3.  The Bacterial ClpXP-ClpB Family Is Enriched with RNA-Binding Protein Complexes.

Authors:  Georg Auburger; Jana Key; Suzana Gispert
Journal:  Cells       Date:  2022-08-02       Impact factor: 7.666

Review 4.  Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries.

Authors:  Abdullah Al Mutery; Mona Mahfood; Jihen Chouchen; Abdelaziz Tlili
Journal:  Hum Genet       Date:  2021-08-02       Impact factor: 4.132

5.  Two Novel Pathogenic Variants Confirm RMND1 Causative Role in Perrault Syndrome with Renal Involvement.

Authors:  Dominika Oziębło; Joanna Pazik; Iwona Stępniak; Henryk Skarżyński; Monika Ołdak
Journal:  Genes (Basel)       Date:  2020-09-08       Impact factor: 4.096

6.  Perrault syndrome: Clinical report and retrospective analysis.

Authors:  Zhaoyu Pan; Hongen Xu; Yongan Tian; Danhua Liu; Huanfei Liu; Ruijun Li; Qian Dou; Bin Zuo; Rongqun Zhai; Wenxue Tang; Wei Lu
Journal:  Mol Genet Genomic Med       Date:  2020-08-07       Impact factor: 2.183

  6 in total

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