Literature DB >> 4375505

Genetic forms of pituitary dwarfism.

D L Rimoin.   

Abstract

Pituitary dwarfism represents a genetically heterogeneous group of disorders which may be classified on the basis of: associated developmental anomalies or degenerative disease; deficiency of, or peripheral insensitivity to HGH; the number of deficient hormones; the associated metabolic disturbances; and the mode of inheritance. Hereditary forms of pituitary dwarfism include: congenital absence of the pituitary, panhypopituitary dwarfism (autosomal and X-linked recessive forms), isolated HGH deficiency (Types I and II), Laron type of dwarfism, and peripheral unresponsiveness to HGH (the African Pygmies).

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Year:  1971        PMID: 4375505

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  2 in total

1.  X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

Authors:  M Lagerström-Fermér; M Sundvall; E Johnsen; G L Warne; S M Forrest; J D Zajac; A Rickards; D Ravine; U Landegren; U Pettersson
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

2.  [Familial panhypopituitarism].

Authors:  D Hamann; T Olbricht; B P Hauffa; D Reinwein
Journal:  Klin Wochenschr       Date:  1991-10-02
  2 in total

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