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J Pediatr Endocrinol Metab ; 28(9-10): 1005-7, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25741941

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.


Subject(s)
Dwarfism, Pituitary/complications , Gonadal Dysgenesis, 46,XX/complications , Hearing Loss, Sensorineural/complications , Human Growth Hormone/deficiency , Adolescent , Dwarfism, Pituitary/genetics , Female , Gonadal Dysgenesis, 46,XX/genetics , Hearing Loss, Sensorineural/genetics , Humans
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