Literature DB >> 12942181

[The Levy-Hollister syndrome: a syndrome of dysplasias with ENT-manifestations].

O Fierek1, R Laskawi, C Bönnemann, F Hanefeld.   

Abstract

The Levy-Hollister syndrome is characterized by a highly variable expression of dysplasia in different organ systems. Autosomal-dominant inheritance is recognised, but most cases are sporadic. In the field of otorhinolaryngology, xerostomia can be found due to aplasia of the major salivary glands, as well as congenital sensorineural, conductive or combined hearing loss and dysplasia of the auricles, mostly appearing as cup-shaped ears. Here we report on a 2-year-old boy with severe xerostomia. The disease was found to be caused by bilateral aplasia of the parotid and submandibular glands. There were also slight dysplasias of both auricles and a bilateral inner ear malformation as the origin of sensorineural hearing loss. Due to its highly variable expression, Levy-Hollister syndrome is often difficult to distinguish from other diseases and syndromes, so that the cooperation of different departments is necessary for an accurate diagnosis. Because of its dominant inheritance, a genetic consultation should be recommended to the patient. Auricular dysplasia and conductive hearing loss can possibly be treated surgically.

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Year:  2003        PMID: 12942181     DOI: 10.1007/s00106-002-0779-5

Source DB:  PubMed          Journal:  HNO        ISSN: 0017-6192            Impact factor:   1.284


  16 in total

Review 1.  The p63 gene in EEC and other syndromes.

Authors:  H G Brunner; B C J Hamel; H Van Bokhoven
Journal:  J Med Genet       Date:  2002-06       Impact factor: 6.318

Review 2.  Monolateral aplasia of the parotid gland.

Authors:  G Almadori; F Ottaviani; M Del Ninno; G Cadoni; G De Rossi; G Paludetti
Journal:  Ann Otol Rhinol Laryngol       Date:  1997-06       Impact factor: 1.547

3.  LADD syndrome: a distinct entity?

Authors:  R C Hennekam
Journal:  Eur J Pediatr       Date:  1987-01       Impact factor: 3.183

4.  Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome. Its association with conductive hearing loss.

Authors:  G C Robinson; L S Wildervanck; T P Chiang
Journal:  J Pediatr       Date:  1973-01       Impact factor: 4.406

5.  Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromes.

Authors:  D Lacombe; F Serville; D Marchand; J Battin
Journal:  J Med Genet       Date:  1993-08       Impact factor: 6.318

6.  [Branchio-oto-renal syndrome (BOR syndrome). A dysplasia syndrome with branchial abnormalities, deafness and kidney disease].

Authors:  M Holzmüller
Journal:  HNO       Date:  2000-11       Impact factor: 1.284

7.  Mesoectodermal dysplasia. A new combination of anomalies.

Authors:  W J Levy
Journal:  Am J Ophthalmol       Date:  1967-05       Impact factor: 5.258

8.  The Lacrimo-Auriculo-Dento-Digital (LADD) syndrome: temporal bone CT findings.

Authors:  M M Lemmerling; B D Vanzieleghem; I J Dhooge; P B Van Cauwenberge; M F Kunnen
Journal:  J Comput Assist Tomogr       Date:  1999 May-Jun       Impact factor: 1.826

9.  Epiglottic hypoplasia associated with lacrimo-auriculo-dental-digital syndrome.

Authors:  T Azar; J A Scott; J E Arnold; N H Robin
Journal:  Ann Otol Rhinol Laryngol       Date:  2000-08       Impact factor: 1.547

Review 10.  Levy-Hollister syndrome.

Authors:  J M Kreutz; H E Hoyme
Journal:  Pediatrics       Date:  1988-07       Impact factor: 7.124

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  1 in total

1.  Lacrimo-auriculo-dento-digital syndrome: A case report and literature review.

Authors:  Reem Alhamadi; Sahar M Elkhamary; Azza Maktabi; Hamad M AlSulaiman; Silvana A Schellini
Journal:  Saudi J Ophthalmol       Date:  2022-02-18
  1 in total

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