Literature DB >> 7277424

The Patterson syndrome, leprechaunism, and pseudoleprechaunism.

T J David, B W Webb, I R Gordon.   

Abstract

A bizarre syndrome has hitherto masqueraded as leprechaunism, and although it is a quite different disorder it has been used as the prototype of leprechaunism in some birth defects atlases. It is proposed that this condition is designated the Patterson syndrome and details of a second case are reported. The features of this connective tissue and neuroendocrine disorder include bronzed hyperpigmentation, cutis laxa of the hands and feet, bodily disproportion, severe mental retardation, and major bony deformities. Radiographs revealed a unique and gross generalised skeletal dysplasia, unlikely to be confused with any other disorder. This endocrine abnormality comprised hyperadrenocorticism, cushingoid features, and diabetes mellitus in the first case, and premature adrenarche in the second case. The pathogenesis and aetiology of the Patterson syndrome are unknown, although quantitative and qualitative abnormalities of mucopolysaccharide excretion were found in the second case.

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Year:  1981        PMID: 7277424      PMCID: PMC1048735          DOI: 10.1136/jmg.18.4.294

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


  10 in total

1.  DYSTROPHIC CHANGES ASSOCIATED WITH LEPRECHAUNISM IN A MALE INFANT.

Authors:  M A SALMON; J N WEBB
Journal:  Arch Dis Child       Date:  1963-10       Impact factor: 3.791

2.  Leprechaunism.

Authors:  P R EVANS
Journal:  Arch Dis Child       Date:  1955-12       Impact factor: 3.791

3.  Leprechaunism: a euphemism for a rare familial disorder.

Authors:  W L DONOHUE; I UCHIDA
Journal:  J Pediatr       Date:  1954-11       Impact factor: 4.406

4.  Leprechaunism in a male infant.

Authors:  J H PATTERSON; W L WATKINS
Journal:  J Pediatr       Date:  1962-05       Impact factor: 4.406

5.  A unique chondrodysplasia secondary to a defect in chondroosseous transformation.

Authors:  J Zonana; D L Rimoin; R S Lachman; A H Cohen
Journal:  Birth Defects Orig Artic Ser       Date:  1977

6.  A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance.

Authors:  L Dallaire; M Cantin; S B Melançon; G Perreault; M Potier
Journal:  Clin Genet       Date:  1976-07       Impact factor: 4.438

7.  Metaphyseal chondrodysplasia calcificans. A report on two cases.

Authors:  S van Creveld; K Kozlowski; K Pietron; A van der Valk
Journal:  Br J Radiol       Date:  1971-10       Impact factor: 3.039

8.  "New" dwarfing syndromes.

Authors:  J Spranger
Journal:  Birth Defects Orig Artic Ser       Date:  1977

9.  A case of leprechaunism with severe hyperinsulinemia.

Authors:  A M Rosenberg; J C Haworth; G W Degroot; C L Trevenen; M M Rechler
Journal:  Am J Dis Child       Date:  1980-02

10.  Leprechaunism (Donohue's syndrome): a case report.

Authors:  R L Summitt; B E Favara
Journal:  J Pediatr       Date:  1969-04       Impact factor: 4.406

  10 in total
  3 in total

1.  Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia.

Authors:  G A Wallis; B Rash; B Sykes; J Bonaventure; P Maroteaux; B Zabel; R Wynne-Davies; M E Grant; R P Boot-Handford
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

2.  A syndrome of insulin resistance resembling leprechaunism in five sibs of consanguineous parents.

Authors:  L I al-Gazali; M Khalil; K Devadas
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

3.  Group B streptococcus meningitis in a child with cochlear implant.

Authors:  Daniel Glikman; Michal Luntz; Rabia Shihada; Zeev Zonis; Lea Even
Journal:  Emerg Infect Dis       Date:  2009-10       Impact factor: 6.883

  3 in total

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