Literature DB >> 25741941

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

Ritesh K Agrawala, Arun K Choudhury, Binoy K Mohanty, Anoj K Baliarsinha.   

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.

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Year:  2015        PMID: 25741941     DOI: 10.1515/jpem-2014-0292

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  1 in total

1.  Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Authors:  R Faridi; A U Rehman; R J Morell; P L Friedman; L Demain; S Zahra; A A Khan; D Tohlob; M Z Assir; G Beaman; S N Khan; W G Newman; S Riazuddin; T B Friedman
Journal:  Clin Genet       Date:  2016-11-16       Impact factor: 4.438

  1 in total

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