Literature DB >> 15868129

[Sensorineural hearing loss in LEOPARD syndrome].

T Schrom1, A Habermann, H Scherer.   

Abstract

The rare multiple lentigines (LEOPARD) syndrome represents a complex of skin, cardiac, skeletal, inner ear and other malformations. There is marked variability in expression of the syndrome. We report on a 20 year old man, showing typical lentiginosis, a retardation of growth, tachycardiac conduction abnormality, ophthalmologic manifestations and a sensorineural hearing loss. Pathogenesis, clinical and differential diagnostic aspects are discussed in this case report. The early diagnosis of a senosorineural hearing loss is useful in order to provide appropriate rehabilitation. When lentiginosis is diagnosed, it is important to consider further abnormalities such as cardiomyopathy, which can be associated with a high mortality.

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Year:  2006        PMID: 15868129     DOI: 10.1007/s00106-005-1265-7

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


  18 in total

1.  Leopard syndrome.

Authors:  S Shamsadini; H Abazardi; F Shamsadini
Journal:  Lancet       Date:  1999-10-30       Impact factor: 79.321

2.  [Progressive cardiomyopathic lentiginosis].

Authors:  M Hug; E Krammer; J L Fischer; L Henselmann
Journal:  Z Kardiol       Date:  1998-02

Review 3.  LEOPARD syndrome (cardiocutaneous lentiginosis syndrome).

Authors:  S Józwiak; R A Schwartz; C K Janniger
Journal:  Cutis       Date:  1996-04

4.  An intriguing case of LEOPARD syndrome.

Authors:  C Schepis; D Greco; M Siragusa; D Batolo; C Romano
Journal:  Pediatr Dermatol       Date:  1998 Mar-Apr       Impact factor: 1.588

5.  Multiple lentigenes syndrome.

Authors:  R J Gorlin; R C Anderson; M Blaw
Journal:  Am J Dis Child       Date:  1969-06

6.  [The leopard syndrome, a cardio-cutaneous syndrome].

Authors:  W Jurecka; W Gebhart; R Knobler; R Schmoliner; H Möslacher
Journal:  Wien Klin Wochenschr       Date:  1983-09-30       Impact factor: 1.704

7.  [Multiple lentigines syndrome (LEOPARD syndrome)].

Authors:  P Dorittke
Journal:  Kinderkrankenschwester       Date:  1992-06

8.  PTPN11 mutations in LEOPARD syndrome.

Authors:  E Legius; C Schrander-Stumpel; E Schollen; C Pulles-Heintzberger; M Gewillig; J-P Fryns
Journal:  J Med Genet       Date:  2002-08       Impact factor: 6.318

9.  [Molecular genetic mutation analysis of the PTPN11 gene in the multiple lentigines (LEOPARD) syndrome].

Authors:  U G Froster; H-J Glander; W Heinritz
Journal:  Hautarzt       Date:  2003-12       Impact factor: 0.751

10.  Diffuse lentiginosis in a patient with Werner's syndrome--a possible association with incomplete leopard syndrome.

Authors:  A Lazarov; E Finkelstein; I Avinoach; L Kachko; S Halevy
Journal:  Clin Exp Dermatol       Date:  1995-01       Impact factor: 3.470

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