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