JOURNAL OF SHANGHAI JIAOTONG UNIVERSITY (MEDICAL SCIENCE)

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Report of 3 cases of 47,XXX syndrome with growth retardatio

YANG Li, FENG Ya-qin, YANG Yu, XIE Li-ling, WANG Di-lan, HUANG Hui   

  • Received:2021-03-31 Published:2021-10-22
  • Contact: YANG Yu, E-mail: yangyu5168@126.com.
  • Supported by:
    None

Abstract: To analyze the clinical data of 3 children with growth retardation, including height, chromosome karyotype, and the levels of growth hormone, insulin-like growth factor-1 and gonadal development. All the 3 cases of children were found to be slow in growth rate, no special face, and normal level of insulin-like growth factor-1; the 3 cases all underwent growth hormone provocation test, of which 1 case was partial growth hormone deficiency and 2 cases were idiopathic short; 3 cases of chromosomal karyotypes were 47, XXX, in line with the diagnosis of super-female syndrome.

Key words: 47,XXX syndrome, growth retardation, chromosomal disease, child

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