Literature DB >> 1261064

Cardio-cutaneous syndrome (the "LEOPARD" syndrome). Review of the literature and a new family.

H Seuanez, F Mañe-Garzon, R Kolski.   

Abstract

Numerous reports of familial cardiac disorders associated with abnormalities of cutaneous pigmentation have appeared in the literature. In some of these there have been other somatic malformations including retardation of growth and anomalous development of the genitalia. In this paper we review the literature and describe another family with multiple lentigines occurring in six members out of eight examined. They were reported to occur in 10 other members not seen by us. The trait showed an autosomal dominant mode of inheritance and appeared to be transmitted by affected fathers. In previous reports transmission has usually been through an affected mother. In five of the six patients examined, only skin abnormalities were detected, but in the propositus the lentigines were associated with retardation of growth, hypertelorism, abnormal genitalia and complete atrioventricular block. The possible explanations for the lack of pleomorphy in other members of the family are discussed.

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Year:  1976        PMID: 1261064     DOI: 10.1111/j.1399-0004.1976.tb01574.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

1.  Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis).

Authors:  B D Coppin; I K Temple
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  Werner's syndrome.

Authors:  G Rosenthal; V Assa; T Monos; B Biedner; T Lifshitz; H Zirkin; E Finkelstein; A Lazarov
Journal:  Br J Ophthalmol       Date:  1996-06       Impact factor: 4.638

3.  Bilateral combined hamartoma of the retina and the retinal pigment epithelium.

Authors:  J H Meyer; H Witschel
Journal:  Br J Ophthalmol       Date:  1996-06       Impact factor: 4.638

4.  Premature cataracts associated with generalized lentigo.

Authors:  R O Howard
Journal:  Trans Am Ophthalmol Soc       Date:  1979

5.  Syndromic Hearing Loss in Association with PTPN11-Related Disorder: The Experience of Cochlear Implantation in a Child with LEOPARD Syndrome.

Authors:  Ho-Suk Chu; Hae-Sun Chung; Moon-Hee Ko; Hee-Jin Kim; Chang-Seok Ki; Won-Ho Chung; Yang-Sun Cho; Sung Hwa Hong
Journal:  Clin Exp Otorhinolaryngol       Date:  2011-02-07       Impact factor: 3.372

6.  Familial pulmonary valve stenosis, atrial septal defect, and unique electrocardiogram abnormalities.

Authors:  A A Ciuffo; E Cunningham; T A Traill
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

7.  Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

Authors:  C A Stratakis; J A Carney; J P Lin; D A Papanicolaou; M Karl; D L Kastner; E Pras; G P Chrousos
Journal:  J Clin Invest       Date:  1996-02-01       Impact factor: 14.808

  7 in total

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