Literature DB >> 1248181

Cerebellar ataxia and hypergonadotropic hypogonadism in two kindreds. Chance concurrence, pleiotropism or linkage?

H Skre, H H Bassöe, K Berg, A G Frövig.   

Abstract

Two kindreds with Marinesco-Sjögren's syndrome in three sibships are described. In five of the six affected, but in none of the unaffected sibs, a hypergonadotropic hypogonadism was observed. In one of the kindreds a high degree of inbreeding was revealed, and inbreeding likely also existed in the other kindred. The two families were not related. Marinesco-Sjögren's syndrome is known to be a distinct clinical entity, governed by autosomal recessive inheritance, and this also applies to hypergonadotropic hypogonadism. Several heredo-degenerative nervous disorders are accompanied by a hypogonadotropic hypogonadism, which is believed to be secondary to the neurological disorder, as in traumatic paraplegia. A hypergonadotropic hypoganadism cannot readily be explained in this way. We consider genetic linkage between two independent disorders as the most likely explanation for the observed concurrence.

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Year:  1976        PMID: 1248181     DOI: 10.1111/j.1399-0004.1976.tb01570.x

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


  6 in total

1.  Two adult females with a distinct familial mental retardation syndrome: non-progressive neurological symptoms with ataxia and hypotonia, similar facial appearance, hypergonadotrophic hypogonadism, and retinal dystrophy.

Authors:  J P Fryns; C Van Lingen; K Devriendt; E Legius; P Raus
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

2.  Martsolf syndrome in a brother and sister: clinical features and pattern of inheritance.

Authors:  R C Hennekam; A G van de Meeberg; J M van Doorne; P F Dijkstra; J B Bijlsma
Journal:  Eur J Pediatr       Date:  1988-06       Impact factor: 3.183

3.  Familial cerebellar ataxia with hypogonadism.

Authors:  A Lowenthal; J Bekaert; F Van Dessel; J van Hauwaert
Journal:  J Neurol       Date:  1979       Impact factor: 4.849

4.  Hereditary ectodermal dysplasia, olivopontocerebellar degeneration, short stature, and hypogonadism.

Authors:  A R Rushton; M Genel
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

5.  Syndrome of cerebellar ataxia and hypogonadotrophic hypogonadism: evidence for pituitary gonadotrophin deficiency.

Authors:  A C Fok; M C Wong; J S Cheah
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-03       Impact factor: 10.154

Review 6.  Primary ovarian insufficiency: an update.

Authors:  Leticia Cox; James H Liu
Journal:  Int J Womens Health       Date:  2014-02-20
  6 in total

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