Literature DB >> 27170934

Diagnosis of osteopetrosis in bilateral congenital aural atresia: Turning point in treatment strategy.

Ritu Verma1, Manisha Jana1, Ashu Seith Bhalla1, Arvind Kumar1, Rakesh Kumar1.   

Abstract

Aural atresia is a rare congenital malformation of the external and middle ear. There are several syndromic associations of this anomaly with those involving the first and second branchial arches. Occurrence of aural atresia with sclerosing skeletal dysplasia is unknown and has never been reported. The co-existence of a sclerosing dysplasia can make the surgical treatment in aural atresia difficult and risky; and the auditory improvement may not be as expected. Moreover, internal auditory canal narrowing and hence sensorineural hearing loss in sclerosing dysplasia might add to the already existing conductive hearing loss in such patients. In this case report we have described an unknown association of bilateral microtia with sclerosing skeletal dysplasia (autosomal dominant osteopetrosis) and clinical implications of these two conditions occurring together leading to a change in the management plan.

Entities:  

Keywords:  Aural atresia; Congenital hearing loss; Microtia; Osteopetrosis

Year:  2016        PMID: 27170934      PMCID: PMC4857237          DOI: 10.5409/wjcp.v5.i2.228

Source DB:  PubMed          Journal:  World J Clin Pediatr        ISSN: 2219-2808


  11 in total

1.  Preoperative evaluation of external auditory canal atresia on high-resolution CT.

Authors:  Eva Maria Gassner; Ammar Mallouhi; Werner R Jaschke
Journal:  AJR Am J Roentgenol       Date:  2004-05       Impact factor: 3.959

2.  Type II autosomal dominant osteopetrosis (Albers-Schönberg disease): clinical and radiological manifestations in 42 patients.

Authors:  O D Bénichou; J D Laredo; M C de Vernejoul
Journal:  Bone       Date:  2000-01       Impact factor: 4.398

3.  Measurement of tartrate-resistant acid phosphatase and the brain isoenzyme of creatine kinase accurately diagnoses type II autosomal dominant osteopetrosis but does not identify gene carriers.

Authors:  Steven G Waguespack; Siu L Hui; Kenneth E White; Kenneth A Buckwalter; Michael J Econs
Journal:  J Clin Endocrinol Metab       Date:  2002-05       Impact factor: 5.958

Review 4.  Genetics of microtia and associated syndromes.

Authors:  F Alasti; G Van Camp
Journal:  J Med Genet       Date:  2009-03-16       Impact factor: 6.318

Review 5.  Osteopetrosis.

Authors:  Zornitza Stark; Ravi Savarirayan
Journal:  Orphanet J Rare Dis       Date:  2009-02-20       Impact factor: 4.123

6.  Preferential associated anomalies in 818 cases of microtia in South America.

Authors:  Daniela V Luquetti; Timothy C Cox; Jorge Lopez-Camelo; Maria da Graça Dutra; Michael L Cunningham; Eduardo E Castilla
Journal:  Am J Med Genet A       Date:  2013-03-29       Impact factor: 2.802

7.  Epidemiology and genetics of microtia-anotia: a registry based study on over one million births.

Authors:  P Mastroiacovo; C Corchia; L D Botto; R Lanni; G Zampino; D Fusco
Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

8.  CT evaluation of congenital aural atresia: what the radiologist and surgeon need to know.

Authors:  J W Yeakley; R A Jahrsdoerfer
Journal:  J Comput Assist Tomogr       Date:  1996 Sep-Oct       Impact factor: 1.826

9.  Malignant infantile osteopetrosis: otolaryngological complications and management.

Authors:  R M Stocks; W C Wang; J W Thompson; M C Stocks; E M Horwitz
Journal:  Arch Otolaryngol Head Neck Surg       Date:  1998-06

10.  HRCT evaluation of microtia: A retrospective study.

Authors:  Aruna R Patil; Ashu Bhalla; Pankaj Gupta; Deepali Goyal; Sreenivas Vishnubhatla; Anurag Ramavat; Suresh Sharma
Journal:  Indian J Radiol Imaging       Date:  2012-07
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