Literature DB >> 6782211

The Cohen syndrome: clinical and endocrinological studies of two new cases.

P Balestrazzi, L Corrini, G Villani, M P Bolla, F Casa, S Bernasconi.   

Abstract

This report concerns two new cases of the Cohen syndrome and gives further information on the variable phenotypical pattern of the disease. The frequency of major and minor clinical signs is reviewed from all the published reports. Among the minor signs we found previously undescribed skeletal abnormalities in one of our patients. The reported delay onset of puberty, which appears to be a frequent aspect of the syndrome, seems to occur without LH and FSH deficiency, as our patients show.

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Year:  1980        PMID: 6782211      PMCID: PMC1885916          DOI: 10.1136/jmg.17.6.430

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  4 in total

1.  [Heterogenity of the cryptorchid syndrome. Study of the pituitary gonadotropin reserve in 50 prepuberal bodys].

Authors:  J Battin; M Colle
Journal:  Arch Fr Pediatr       Date:  1977 Aug-Sep

2.  A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies.

Authors:  M M Cohen; B D Hall; D W Smith; C B Graham; K J Lampert
Journal:  J Pediatr       Date:  1973-08       Impact factor: 4.406

3.  [Heterogeneity of the pituitary reserve of gonadotropins in children with cryptorchism].

Authors:  S Bernasconi; M Vanelli; M Rocca; M Mattioli; G Nori; A Cantarelli; D Ferrara
Journal:  Minerva Pediatr       Date:  1979-11-30       Impact factor: 1.312

4.  Confirmation of the Cohen syndrome.

Authors:  J C Carey; B D Hall
Journal:  J Pediatr       Date:  1978-08       Impact factor: 4.406

  4 in total
  5 in total

1.  Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome.

Authors:  K E Chandler; A Kidd; L Al-Gazali; J Kolehmainen; A-E Lehesjoki; G C M Black; J Clayton-Smith
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

2.  The clinical features of the Cohen syndrome: further case reports.

Authors:  C North; M A Patton; M Baraitser; R M Winter
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

3.  Intrafamilial variation in Cohen syndrome.

Authors:  I D Young; J R Moore
Journal:  J Med Genet       Date:  1987-08       Impact factor: 6.318

4.  Mental retardation, hypotonia, obesity, ocular, facial, dental, and limb abnormalities (Cohen syndrome). Report of three patients.

Authors:  T Goecke; F Majewski; K D Kauther; U Sterzel
Journal:  Eur J Pediatr       Date:  1982-07       Impact factor: 3.183

5.  Growth hormone deficiency in a girl with the Cohen syndrome.

Authors:  G Massa; L Dooms; M Vanderschueren-Lodeweyckx
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

  5 in total

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