Literature DB >> 6507471

Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.

R E Tipton, R J Gorlin.   

Abstract

The GAPO syndrome is a rare but distinct autosomal-recessive disorder. The term GAPO is an acronym for the manifestations of Growth retardation. Alopecia, Pseudo- anodontia (failure of tooth eruption), and progressive Optic atrophy. We are aware of five other published patients. All have a strikingly similar appearance. This, along with other distinct manifestations, should allow clear differentiation from other causes of growth retardation. The hypothesis of autosomal-recessive inheritance is based on parental consanguinity and affected sibs in several cases.

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Year:  1984        PMID: 6507471     DOI: 10.1002/ajmg.1320190202

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  16 in total

1.  Acquired alopecia, mental retardation, short stature, microcephaly, and optic atrophy.

Authors:  R C Hennekam; E G Renckens-Wennen
Journal:  J Med Genet       Date:  1990-10       Impact factor: 6.318

2.  GAPO syndrome with craniosynostosis and intracranial hypertension.

Authors:  Mehdi Golpayegani; Farhad Salari; Zohreh Habibi; Negin Naderian; Farideh Nejat
Journal:  Childs Nerv Syst       Date:  2019-06-23       Impact factor: 1.475

3.  New ANTXR1 Gene Mutation for GAPO Syndrome: A Case Report.

Authors:  Julio C Salas-Alanís; Claire A Scott; Oscar R Fajardo-Ramírez; Carola Duran; María G Moreno-Treviño; David P Kelsell
Journal:  Mol Syndromol       Date:  2016-06-02

4.  A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis.

Authors:  Nuriye Dinckan; Renqian Du; Zeynep C Akdemir; Yavuz Bayram; Shalini N Jhangiani; Harsha Doddapaneni; Jianhong Hu; Donna M Muzny; Yeliz Guven; Oya Aktoren; Hulya Kayserili; Eric Boerwinkle; Richard A Gibbs; Jennifer E Posey; James R Lupski; Zehra O Uyguner; Ariadne Letra
Journal:  Am J Med Genet A       Date:  2018-02-13       Impact factor: 2.802

5.  Cell autonomous ANTXR1-mediated regulation of extracellular matrix components in primary fibroblasts.

Authors:  Kai Hu; Bjorn R Olsen; Tatiana Y Besschetnova
Journal:  Matrix Biol       Date:  2016-12-20       Impact factor: 11.583

6.  Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome.

Authors:  Yavuz Bayram; Davut Pehlivan; Ender Karaca; Tomasz Gambin; Shalini N Jhangiani; Serkan Erdin; Claudia Gonzaga-Jauregui; Wojciech Wiszniewski; Donna Muzny; Nursel H Elcioglu; M Selman Yildirim; Banu Bozkurt; Ayse Gul Zamani; Eric Boerwinkle; Richard A Gibbs; James R Lupski
Journal:  Am J Med Genet A       Date:  2014-07-14       Impact factor: 2.802

Review 7.  Cranioectodermal dysplasia (Sensenbrenner's syndrome).

Authors:  I D Young
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

8.  Mutations in ANTXR1 cause GAPO syndrome.

Authors:  Viktor Stránecký; Alexander Hoischen; Hana Hartmannová; Maha S Zaki; Amit Chaudhary; Enrique Zudaire; Lenka Nosková; Veronika Barešová; Anna Přistoupilová; Kateřina Hodaňová; Jana Sovová; Helena Hůlková; Lenka Piherová; Jayne Y Hehir-Kwa; Deepthi de Silva; Manouri P Senanayake; Sameh Farrag; Jiří Zeman; Pavel Martásek; Alice Baxová; Hanan H Afifi; Brad St Croix; Han G Brunner; Samia Temtamy; Stanislav Kmoch
Journal:  Am J Hum Genet       Date:  2013-04-18       Impact factor: 11.025

9.  RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome.

Authors:  Lina Basel-Vanagaite; Ofer Sarig; Dov Hershkovitz; Dana Fuchs-Telem; Debora Rapaport; Andrea Gat; Gila Isman; Idit Shirazi; Mordechai Shohat; Claes D Enk; Efrat Birk; Jürgen Kohlhase; Uta Matysiak-Scholze; Idit Maya; Carlos Knopf; Anette Peffekoven; Hans-Christian Hennies; Reuven Bergman; Mia Horowitz; Akemi Ishida-Yamamoto; Eli Sprecher
Journal:  Am J Hum Genet       Date:  2009-07-23       Impact factor: 11.025

10.  GAPO syndrome with pansutural craniosynostosis leading to intracranial hypertension.

Authors:  Nishant Goyal; Hitesh Gurjar; Bhawani Shankar Sharma; Manjari Tripathi; P Sarat Chandra
Journal:  BMJ Case Rep       Date:  2014-01-28
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