Literature DB >> 22043478

The male phenotype in osteopathia striata congenita with cranial sclerosis.

Sarah K Holman1, Phil Daniel, Zandra A Jenkins, Rachel L Herron, Tim Morgan, Ravi Savarirayan, C W Chow, Axel Bohring, Annette Mosel, Didier Lacombe, Bernhard Steiner, Thomas Schmitt-Mechelke, Barbara Schroter, Annick Raas-Rothschild, Sixto Garcia Miñaur, Mary Porteous, Michael Parker, Oliver Quarrell, Dagmar Tapon, Valérie Cormier-Daire, Sahar Mansour, Ruth Nash, Laurence A Bindoff, Torunn Fiskerstrand, Stephen P Robertson.   

Abstract

Osteopathia striata with cranial sclerosis (OSCS) is an X-linked disease caused by truncating mutations in WTX. Females exhibit sclerotic striations on the long bones, cranial sclerosis, and craniofacial dysmorphism. Males with OSCS have significant skeletal sclerosis, do not have striations but do display a more severe phenotype commonly associated with gross structural malformations, patterning defects, and significant pre- and postnatal lethality. The recent description of mutations in WTX underlying OSCS has led to the identification of a milder, survivable phenotype in males. Individuals with this presentation can have, in addition to skeletal sclerosis, Hirschsprung disease, joint contractures, cardiomyopathy, and neuromuscular anomalies. A diagnosis of OSCS should be considered in males with macrocephaly, skeletal sclerosis that is most marked in the cranium and the absence of metaphyseal striations. The observation of striations in males may be indicative of a WTX mutation in a mosaic state supporting the contention that this sign in females is indicative of the differential lyonization of cells in the osteoblastic lineage.

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Year:  2011        PMID: 22043478     DOI: 10.1002/ajmg.a.34178

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


  5 in total

1.  Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger.

Authors:  Hiroko Yagi; Masaki Takagi; Yukihiro Hasegawa; Hülya Kayserili; Gen Nishimura
Journal:  Pediatr Radiol       Date:  2015-04-03

Review 2.  WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features.

Authors:  Anna Maria Zicari; Luigi Tarani; Daniela Perotti; Laura Papetti; Francesco Nicita; Natascia Liberati; Alberto Spalice; Guglielmo Salvatori; Federica Guaraldi; Marzia Duse
Journal:  Ital J Pediatr       Date:  2012-06-20       Impact factor: 2.638

3.  Whole Exome Sequencing Provides the Correct Diagnosis in a Case of Osteopathia Striata with Cranial Sclerosis: Case Report of a Novel Frameshift Mutation in AMER1.

Authors:  José María García-Aznar; Noelia Ramírez; David De Uña; Elisa Santiago; Lorenzo Monserrat
Journal:  J Pediatr Genet       Date:  2020-04-21

4.  Deletion of Exon 1 in AMER1 in Osteopathia Striata with Cranial Sclerosis.

Authors:  Jingyi Mi; Padmini Parthasarathy; Benjamin J Halliday; Tim Morgan; John Dean; Malgorzata J M Nowaczyk; David Markie; Stephen P Robertson; Emma M Wade
Journal:  Genes (Basel)       Date:  2020-11-30       Impact factor: 4.096

5.  Mosaic Deletions of Known Genes Explain Skeletal Dysplasias With High and Low Bone Mass.

Authors:  Mari Muurinen; Fulya Taylan; Symeon Tournis; Jesper Eisfeldt; Alexia Balanika; Heleni Vastardis; Sirpa Ala-Mello; Outi Mäkitie; Alice Costantini
Journal:  JBMR Plus       Date:  2022-07-05
  5 in total

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