Literature DB >> 28486374

Premature Thelarche and the PURA Syndrome.

Joshua Rezkalla1, Tiffany Von Wald, Keith A Hansen.   

Abstract

BACKGROUND: Premature thelarche is a self-limited condition characterized by Tanner stage II-III breast development in girls younger than 8 years of age with no evidence of advancing puberty. Evaluation concentrates on excluding central or peripheral causes of precocious puberty. CASE: A girl aged 2 years 4 months with profound hypotonia and delayed developmental milestones presented with Tanner II breast development, elevated follicle-stimulating hormone levels, suppressed luteinizing hormone level, normal growth and skeletal development, and prepubertal uterine length and ovarian volume. Monitoring until 8 years of age revealed no pubertal progression. Whole exome sequencing at 8 years revealed an autosomal-dominant mutation in the purine-rich element-binding protein A (PURA) gene. Previous patients with PURA syndrome have had pituitary dysfunction and precocious puberty.
CONCLUSION: Purine-rich element-binding protein A syndrome can be associated with premature thelarche.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28486374     DOI: 10.1097/AOG.0000000000002047

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  5 in total

1.  A novel de novo mutation in the PURA gene associated with a new clinical finding: large brainstem.

Authors:  María Elena Rodríguez-García; Francisco Javier Cotrina-Vinagre; Elena Arranz-Canales; Ana Martínez de Aragón; Laura Hernández-Sánchez; Fátima Rodríguez-Fornés; Patricia Carnicero-Rodríguez; Montserrat Morales-Conejo; Elena Martín-Hernández; Francisco Martínez-Azorín
Journal:  J Genet       Date:  2020       Impact factor: 1.166

2.  Expanding the PURA syndrome phenotype: A child with the recurrent PURA p.(Phe233del) pathogenic variant showing similarities with cutis laxa.

Authors:  Valeria Cinquina; Claudia Ciaccio; Marina Venturini; Riccardo Masson; Marco Ritelli; Marina Colombi
Journal:  Mol Genet Genomic Med       Date:  2020-12-04       Impact factor: 2.183

Review 3.  PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature.

Authors:  Margot R F Reijnders; Robert Janowski; Mohsan Alvi; Jay E Self; Ton J van Essen; Maaike Vreeburg; Rob P W Rouhl; Servi J C Stevens; Alexander P A Stegmann; Jolanda Schieving; Rolph Pfundt; Katinke van Dijk; Eric Smeets; Connie T R M Stumpel; Levinus A Bok; Jan Maarten Cobben; Marc Engelen; Sahar Mansour; Margo Whiteford; Kate E Chandler; Sofia Douzgou; Nicola S Cooper; Ene-Choo Tan; Roger Foo; Angeline H M Lai; Julia Rankin; Andrew Green; Tuula Lönnqvist; Pirjo Isohanni; Shelley Williams; Ilene Ruhoy; Karen S Carvalho; James J Dowling; Dorit L Lev; Katalin Sterbova; Petra Lassuthova; Jana Neupauerová; Jeff L Waugh; Sotirios Keros; Jill Clayton-Smith; Sarah F Smithson; Han G Brunner; Ceciel van Hoeckel; Mel Anderson; Virginia E Clowes; Victoria Mok Siu; The Ddd Study; Paulo Selber; Richard J Leventer; Christoffer Nellaker; Dierk Niessing; David Hunt; Diana Baralle
Journal:  J Med Genet       Date:  2017-11-02       Impact factor: 6.318

4.  Neonatal PURA syndrome: a case report and literature review.

Authors:  Ying Liu; Rui Liu; Tong Xu; Yu-Xin Zhou; Shuang-Chuan Zhang
Journal:  Transl Pediatr       Date:  2021-01

5.  PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum.

Authors:  Katrine M Johannesen; Elena Gardella; Cathrine E Gjerulfsen; Allan Bayat; Rob P W Rouhl; Margot Reijnders; Sandra Whalen; Boris Keren; Julien Buratti; Thomas Courtin; Klaas J Wierenga; Bertrand Isidor; Amélie Piton; Laurence Faivre; Aurore Garde; Sébastien Moutton; Frédéric Tran-Mau-Them; Anne-Sophie Denommé-Pichon; Christine Coubes; Austin Larson; Michael J Esser; Juan Pablo Appendino; Walla Al-Hertani; Beatriz Gamboni; Alejandra Mampel; Lía Mayorga; Alessandro Orsini; Alice Bonuccelli; Agnese Suppiej; Julien Van-Gils; Julie Vogt; Simona Damioli; Lucio Giordano; Stephanie Moortgat; Elaine Wirrell; Sarah Hicks; Usha Kini; Nathan Noble; Helen Stewart; Shailesh Asakar; Julie S Cohen; SakkuBai R Naidu; Ashley Collier; Eva H Brilstra; Mindy H Li; Casey Brew; Stefania Bigoni; Davide Ognibene; Elisa Ballardini; Claudia Ruivenkamp; Raffaella Faggioli; Alexandra Afenjar; Diana Rodriguez; David Bick; Devorah Segal; David Coman; Boudewijn Gunning; Orrin Devinsky; Laurie A Demmer; Theresa Grebe; Dario Pruna; Ida Cursio; Lynn Greenhalgh; Claudio Graziano; Rahul Raman Singh; Gaetano Cantalupo; Marjolaine Willems; Sangeetha Yoganathan; Fernanda Góes; Richard J Leventer; Davide Colavito; Sara Olivotto; Barbara Scelsa; Andrea V Andrade; Kelly Ratke; Farha Tokarz; Atiya S Khan; Clothilde Ormieres; William Benko; Karen Keough; Sotirios Keros; Shanawaz Hussain; Ashlea Franques; Felicia Varsalone; Sabine Grønborg; Cyril Mignot; Delphine Heron; Caroline Nava; Arnaud Isapof; Felippe Borlot; Robyn Whitney; Anne Ronan; Nicola Foulds; Marta Somorai; John Brandsema; Katherine L Helbig; Ingo Helbig; Xilma R Ortiz-González; Holly Dubbs; Antonio Vitobello; Mel Anderson; Dominic Spadafore; David Hunt; Rikke S Møller; Guido Rubboli
Journal:  Neurol Genet       Date:  2021-11-15
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.