Literature DB >> 2309787

A "new" skeletal dysplasia in two unrelated boys.

R A Saul1, W G Wilson.   

Abstract

We report on 2 unrelated boys with similar physical and radiographic findings that may represent a "new" skeletal dysplasia. Findings in common include early speech delay, short stature, frontal bossing with a depression over the metopic suture, a narrow nasal root with beaked nose, midfacial hypoplasia with relatively prominent eyes, and brachydactyly with blunt fingers. Radiographic findings include mild irregularities of the vertebral bodies, hypoplasia of the odontoid process, short phalanges with increased distal width, coning and sclerosis of several epiphyses, and overtubulation of the long bones. Although these patients share some manifestations with the floating-harbor syndrome (Robinson et al.: J Pediatr 113:703-706, 1988), their radiographic changes are distinctive and are not suggestive of a recognized skeletal dysplasia syndrome.

Entities:  

Mesh:

Year:  1990        PMID: 2309787     DOI: 10.1002/ajmg.1320350315

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


  6 in total

1.  A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.

Authors:  Simeon A Boyadjiev; Cristina M Justice; Wafaa Eyaid; Victor A McKusick; Ralph S Lachman; Arnab B Chowdry; Monzer Jabak; Johan Zwaan; Alexander F Wilson; Ethylin Wang Jabs
Journal:  Hum Genet       Date:  2003-04-03       Impact factor: 4.132

2.  A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.

Authors:  Carlos R Ferreira; Zhi-Jie Xia; Aurélie Clément; David A Parry; Mariska Davids; Fulya Taylan; Prashant Sharma; Coleman T Turgeon; Bernardo Blanco-Sánchez; Bobby G Ng; Clare V Logan; Lynne A Wolfe; Benjamin D Solomon; Megan T Cho; Ganka Douglas; Daniel R Carvalho; Heiko Bratke; Marte Gjøl Haug; Jennifer B Phillips; Jeremy Wegner; Michael Tiemeyer; Kazuhiro Aoki; Ann Nordgren; Anna Hammarsjö; Angela L Duker; Luis Rohena; Hanne Buciek Hove; Jakob Ek; David Adams; Cynthia J Tifft; Tito Onyekweli; Tara Weixel; Ellen Macnamara; Kelly Radtke; Zöe Powis; Dawn Earl; Melissa Gabriel; Alvaro H Serrano Russi; Lauren Brick; Mariya Kozenko; Emma Tham; Kimiyo M Raymond; John A Phillips; George E Tiller; William G Wilson; Rizwan Hamid; May C V Malicdan; Gen Nishimura; Giedre Grigelioniene; Andrew Jackson; Monte Westerfield; Michael B Bober; William A Gahl; Hudson H Freeze
Journal:  Am J Hum Genet       Date:  2018-10-04       Impact factor: 11.025

3.  Growth in individuals with Saul-Wilson syndrome.

Authors:  Carlos R Ferreira; Timothy Niiler; Angela L Duker; Andrew P Jackson; Michael B Bober
Journal:  Am J Med Genet A       Date:  2020-07-11       Impact factor: 2.578

4.  Saul-Wilson Syndrome Missense Allele Does Not Show Obvious Golgi Defects in a C. elegans Model.

Authors:  Isabella Zafra; Benjamin Nebenfuehr; Andy Golden
Journal:  MicroPubl Biol       Date:  2021-03-04

5.  A Dominant Heterozygous Mutation in COG4 Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling.

Authors:  Zhi-Jie Xia; Xin-Xin I Zeng; Mitali Tambe; Bobby G Ng; P Duc S Dong; Hudson H Freeze
Journal:  Front Cell Dev Biol       Date:  2021-09-14

6.  Severe Cranio-Cervical Stenosis in a Child with Saul-Wilson Syndrome: A Case Report.

Authors:  Nenad Koruga; Silvija Pušeljić; Višnja Tomac; Anamarija Soldo Koruga; Igor Marjanac; Borna Biljan; Krešimir Šantić; Ivana Lenz; Nora Pušeljić
Journal:  Children (Basel)       Date:  2022-04-08
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.