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Perrault syndrome with growth hormone deficiency: a rare autosomal recessive disorder.

Authors :
Agrawala RK
Choudhury AK
Mohanty BK
Baliarsinha AK
Source :
Journal of pediatric endocrinology & metabolism : JPEM [J Pediatr Endocrinol Metab] 2015 Sep; Vol. 28 (9-10), pp. 1005-7.
Publication Year :
2015

Abstract

Perrault syndrome is a rare genetically heterogeneous autosomal recessive group of disorders described in 1951 by Perrault as gonadal dysgenesis with deafness. Here we present a rare case of sporadic Perrault syndrome with short stature and growth hormone deficiency (GHD). Although there was a report on partial GHD in Perrault, our case is a first of its kind with documented GHD (Nishi Y, Hamamoto K, Kajiyama M, Kawamura I. The Perrault syndrome: clinical report and review. Am J Med Genet 1988;31:623-9). We report this case because of the rarity of keeping this condition as a differential diagnosis while evaluating for short stature with amenorrhea.

Details

Language :
English
ISSN :
2191-0251
Volume :
28
Issue :
9-10
Database :
MEDLINE
Journal :
Journal of pediatric endocrinology & metabolism : JPEM
Publication Type :
Academic Journal
Accession number :
25741941
Full Text :
https://doi.org/10.1515/jpem-2014-0292