Literature DB >> 16010569

Osteopathia striata with cranial sclerosis and hearing loss.

K Lüerssen1, M Ptok.   

Abstract

Osteopathia striata is a manifestation of several bone dysplasias. In association with cranial sclerosis, it represents a separate entity that is not limited to the bones, but may also affect other structures, leading to an abnormal face, cleft palate, deafness, heart defects and vertebral anomalies. Neurological findings range from normal development to marked retardation with hydrocephalus, cranial nerve deficiencies and deafness. So far, only a few patients have been described in the literature, demonstrating autosomal dominant inheritance. Here, we report a spontaneous mutation of inheritance. The parents and three sisters of the affected child are healthy. In 78.6% of the reported cases with osteopathia striata and hearing loss, a conductive hearing loss was described. Surgical attempts to mobilize the middle-ear bones were unsuccessful because of swelling and augmented growth of the bones in the middle ears. Here the mobilization of the eardrum was not attempted because the middle ear cavities were epidermized. This is the second case in the literature in which a myringotomy was not done because the middle ear was completely epidermized. As a possible alternative, children with osteopathia striata and cranial sclerosis with hearing loss should be fitted with hearing aids because surgery of the middle ear probably will be difficult or perhaps not possible.

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Year:  2005        PMID: 16010569     DOI: 10.1007/s00405-005-0972-8

Source DB:  PubMed          Journal:  Eur Arch Otorhinolaryngol        ISSN: 0937-4477            Impact factor:   2.503


  15 in total

1.  Osteopathia striata cranial sclerosis: non-random X-inactivation suggestive of X-linked dominant inheritance.

Authors:  Géraldine Viot; Didier Lacombe; Albert David; Michèle Mathieu; Alain de Broca; Laurence Faivre; Nadine Gigarel; Arnold Munnich; Stanislas Lyonnet; Martine Le Merrer; Valérie Cormier-Daire
Journal:  Am J Med Genet       Date:  2002-01-01

2.  Osteopathia striata, osteopetrosis, and impaired hearing. A case report.

Authors:  M D Jones; N D Mulcahy
Journal:  Arch Otolaryngol       Date:  1968-02

3.  Two cases of osteopathia striata, deafness and cranial osteopetrosis.

Authors:  P P Franklyn; D Wilkinson
Journal:  Ann Radiol (Paris)       Date:  1978 Mar-Apr

4.  Further clinical delineation and increased morbidity in males with osteopathia striata with cranial sclerosis: an X-linked disorder?

Authors:  J E Pellegrino; D M McDonald-McGinn; A Schneider; R I Markowitz; E H Zackai
Journal:  Am J Med Genet       Date:  1997-05-16

5.  Osteopathia striata with cranial sclerosis. An autosomal dominant entity.

Authors:  F T Horan; P H Beighton
Journal:  Clin Genet       Date:  1978-02       Impact factor: 4.438

6.  Severe malformations in males from families with osteopathia striata with cranial sclerosis.

Authors:  A L Bueno; F J Ramos; O Bueno; J L Olivares; M L Bello; M Bueno
Journal:  Clin Genet       Date:  1998-11       Impact factor: 4.438

Review 7.  Multiple malformations in a male and maternal osteopathia strata with cranial sclerosis (OSCS).

Authors:  H D Rott; P Krieg; H Rütschle; C Kraus
Journal:  Genet Couns       Date:  2003

8.  Syndrome of osteopathia striata, macrocephaly, and cranial sclerosis.

Authors:  M Robinow; F Unger
Journal:  Am J Dis Child       Date:  1984-09

9.  Osteopathia striata with cranial sclerosis. Report of a case and review of the literature.

Authors:  J De Keyser; M Bruyland; J De Greve; J Leemans; R Potvliege; R Six; G Ebinger
Journal:  Clin Neurol Neurosurg       Date:  1983       Impact factor: 1.876

Review 10.  Osteopathia striata with cranial sclerosis.

Authors:  B B Gay; L J Elsas; J B Wyly; M Pasquali
Journal:  Pediatr Radiol       Date:  1994
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  1 in total

Review 1.  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

  1 in total

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