Literature DB >> 7215712

Two children with cerebral gigantism and congenital primary hypothyroidism.

J A Hulse.   

Abstract

Two children are described in whom congenital primary hypothyroidism was associated with excessive growth during early childhood and who had typical morphological features of cerebral gigantism. One child was completely athyreotic. This association has been described previously in only one other child.

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Year:  1981        PMID： 7215712     DOI： 10.1111/j.1469-8749.1981.tb02448.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN： 0012-1622            Impact factor:   5.449


  5 in total

1.  Sotos syndrome.

Authors:  T R Cole; H E Hughes
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

2.  Weaver syndrome.

Authors:  T R Cole; N R Dennis; H E Hughes
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

3.  Early treated hypothyroidism: development at 3 years.

Authors:  G Murphy; J A Hulse; D Jackson; P Tyrer; J Glossop; I Smith; D Grant
Journal:  Arch Dis Child       Date:  1986-08       Impact factor: 3.791

4.  Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Authors:  K Zerres; S Rudnik-Schöneborn; F Deget
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

5.  Growth, development, and reassessment of hypothyroid infants diagnosed by screening.

Authors:  J A Hulse; D B Grant; D Jackson; B E Clayton
Journal:  Br Med J (Clin Res Ed)       Date:  1982-05-15
  5 in total

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