Literature DB >> 23813656

Orthopedic manifestations and implications for individuals with Costello syndrome.

Stacey Detweiler1, Mihir M Thacker, Elizabeth Hopkins, Laura Conway, Karen W Gripp.   

Abstract

Costello syndrome is a rare genetic condition caused by heterozygous alterations in HRAS and characterized by multi-system abnormalities. Individuals with Costello syndrome usually present with severe feeding difficulties in infancy, short stature, coarse facial features, increased tumor risks, cardiac and neurological complications, intellectual disability and orthopedic complications. This study further defines the orthopedic manifestations affecting individuals with Costello syndrome. We studied 43 participants and performed medical records review, clinical examinations and orthopedic inquiry forms. In 23 participants, hip and or spinal imaging assessments were completed. Serial radiographs were analyzed when available. A total of 25 orthopedic manifestations were identified. Ten manifestations were seen in the majority of the participants: hypotonia (87%), ligamentous laxity (85%), scoliosis (63%), kyphosis (58%), characteristic hand deformities (85%), ulnar deviation of the wrist (63%), elbow (55%) and shoulder contractures (65%), tight Achilles tendon (73%), and pes planus (53%). Other characteristics of special note were hip dysplasia (45%), foot deformities requiring surgical intervention (38%) and osteopenia/osteoporosis (47%). We also studied the development of the hips and spine. Uni- or bilateral hip dysplasia was congenital in some, while it developed throughout childhood in others. Spinal involvement included scoliosis, kyphosis, lordosis, and curvature reversal (thoracic lordosis and lumbar kyphosis). Based on these findings, we recommend routine referral to an orthopedic surgeon as well as instituting screening protocols for hips and spine for individuals with Costello syndrome.
Copyright © 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  Costello syndrome; HRAS; hip dysplasia; orthopedic manifestations

Mesh:

Year:  2013        PMID: 23813656     DOI: 10.1002/ajmg.a.36047

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  8 in total

1.  Costello syndrome: Clinical phenotype, genotype, and management guidelines.

Authors:  Karen W Gripp; Lindsey A Morse; Marni Axelrad; Kathryn C Chatfield; Aaron Chidekel; William Dobyns; Daniel Doyle; Bronwyn Kerr; Angela E Lin; David D Schwartz; Barbara J Sibbles; Dawn Siegel; Suma P Shankar; David A Stevenson; Mihir M Thacker; K Nicole Weaver; Sue M White; Katherine A Rauen
Journal:  Am J Med Genet A       Date:  2019-06-20       Impact factor: 2.802

2.  Paternal uniparental disomy with segmental loss of heterozygosity of chromosome 11 are hallmark characteristics of syndromic and sporadic embryonal rhabdomyosarcoma.

Authors:  Katherine M Robbins; Deborah L Stabley; Jennifer Holbrook; Rebecca Sahraoui; Alexa Sadreameli; Katrina Conard; Laura Baker; Karen W Gripp; Katia Sol-Church
Journal:  Am J Med Genet A       Date:  2016-09-02       Impact factor: 2.802

3.  Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp.

Authors:  Débora Bertola; Michelle Buscarilli; Deborah L Stabley; Laura Baker; Daniel Doyle; Dennis W Bartholomew; Katia Sol-Church; Karen W Gripp
Journal:  Am J Med Genet A       Date:  2017-04-03       Impact factor: 2.802

4.  Age-related differences in prevalence of autism spectrum disorder symptoms in children and adolescents with Costello syndrome.

Authors:  David D Schwartz; Jennifer M Katzenstein; Eric J Highley; Deborah L Stabley; Katia Sol-Church; Karen W Gripp; Marni E Axelrad
Journal:  Am J Med Genet A       Date:  2017-04-04       Impact factor: 2.802

Review 5.  Multidisciplinary Management of Costello Syndrome: Current Perspectives.

Authors:  Chiara Leoni; Germana Viscogliosi; Marco Tartaglia; Yoko Aoki; Giuseppe Zampino
Journal:  J Multidiscip Healthc       Date:  2022-06-02

6.  Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis.

Authors:  Gang Liu; Hengqiang Zhao; Zihui Yan; Sen Zhao; Yuchen Niu; Xiaoxin Li; Shengru Wang; Yang Yang; Sen Liu; Terry Jianguo Zhang; Zhihong Wu; Nan Wu
Journal:  Mol Ther Nucleic Acids       Date:  2021-02-10       Impact factor: 8.886

7.  Musculo-skeletal phenotype of Costello syndrome and cardio-facio-cutaneous syndrome: insights on the functional assessment status.

Authors:  Antonio Valassina; Giuseppe Zampino; Chiara Leoni; Domenico Marco Romeo; Michele Pelliccioni; Mariangela Di Già; Roberta Onesimo; Valentina Giorgio; Elisabetta Flex; Marta Tedesco; Marco Tartaglia; Donato Rigante
Journal:  Orphanet J Rare Dis       Date:  2021-01-22       Impact factor: 4.123

Review 8.  The skeletal muscle phenotype of children with Neurofibromatosis Type 1 - A clinical perspective.

Authors:  Amish Chinoy; Grace R Vassallo; Emma Burkitt Wright; Judith Eelloo; Siobhan West; Eileen Hupton; Paula Galloway; Amy Pilkington; Raja Padidela; M Zulf Mughal
Journal:  J Musculoskelet Neuronal Interact       Date:  2022-03-01       Impact factor: 1.864

  8 in total

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