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A Weaver‐like syndrome with endocrinological abnormalities in a boy and his mother
Author(s) -
Stoll C.,
Talon P.,
Mengus L.,
Roth M. P.,
Dott B.
Publication year - 1985
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1985.tb00396.x
Subject(s) - galactorrhea , amenorrhea , medicine , pediatrics , endocrinology , primary amenorrhea , growth retardation , pregnancy , prolactin , genetics , hormone , biology
A boy and his mother had dysmorphic features and accelerated growth of prenatal onset suggestive of the Weaver syndrome. Both had endocrinologic abnormalities. The boy had very low, hGH, which did not respond to stimulation. The mother had low, non‐stimulate hGH hyperprolactinemia with secondary amenorrhea and galactorrhea. This is the first report of a mother to son transmission of the condition.