Literature DB >> 6278147

A case of the orocraniodigital (Juberg-Hayward) syndrome.

N C Nevin, P Henry, P T Thomas.   

Abstract

A female with the orocraniodigital (Juberg-Hayward) syndrome is described in whom, in addition to bilateral cleft lip and palate, mild microcephaly, and anomalous thumbs and toes, there was absence of the pituitary fossa and a more widespread skeletal dysplasia.

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Mesh：

Year:  1981        PMID： 6278147      PMCID： PMC1048801          DOI： 10.1136/jmg.18.6.478

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


  1 in total

1.  A new familial syndrome of oral, cranial, and digital anomalies.

Authors:  R C Juberg; J R Hayward
Journal:  J Pediatr       Date:  1969-05       Impact factor: 4.406
  1 in total
  3 in total

Review 1.  The orocraniodigital syndrome of Juberg and Hayward.

Authors:  A Verloes; M Le Merrer; J C Davin; P Wittamer; C Abrassart; G Bricteux; M L Briard
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

2.  Orocraniodigital (Juberg-Hayward) syndrome with growth hormone deficiency.

Authors:  H M Kingston; I A Hughes; P S Harper
Journal:  Arch Dis Child       Date:  1982-10       Impact factor: 3.791

3.  A case with mega cisterna magna renal and ear anomalies: is this a new syndrome?

Authors:  Capan Konca; Bahar Caliskan; Mehmet Ali Tas
Journal:  Case Rep Med       Date:  2013-05-15
  3 in total

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