[Klinefelter syndrome: clinical and auxological features of 14 patients diagnosed in childhood]

Pediatr Med Chir. 2013 Jul-Aug;35(4):183-6. doi: 10.4081/pmc.2013.39.
[Article in Italian]

Abstract

Klinefelter syndrome (KS) is the most frequent chromosomal aneuploidy with a prevalence of 1:500 men but it often remains a largely undiagnosed condition and only 10% of cases are identified in childhood and adolescence. We report the anamnestic, clinical and auxological findings of 14 KS patients diagnosed in paediatric age. 3/14 patients (21%) with KS were diagnosed in prenatal age by amniocentesis, 1 patient was diagnosed at birth due to genital ambiguity and the remaining 10/14 (71.4%) were diagnosed at a chronological age younger than 15 years old for a clinical picture characterized by a peculiar cognitive and behavioral pattern or genital anomalies and abnormalities of pubertal development. The classical karyotype 47 XXY was present in 10/14 subjects (72%), a mosaic form (46 XY/47 XXY) was present in 2/14 (14%) and a complex aneuploidy (48 XXYY and 48 XXXY)was present in the remaining 2/14 (14%) patients. All KS patients diagnosed in childhood and adolescence (10/14 =71.4 %) showed a stature taller than the respective target height and also the predicted final height (calculated from a chronological age older than 7 years old) and the reached final height were significantly taller than target height.

Conclusion: according to our retrospective data we can assert that KS in paediatric age is characterized by a stature taller than target

Publication types

  • English Abstract

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Growth
  • Humans
  • Infant, Newborn
  • Klinefelter Syndrome / diagnosis*
  • Klinefelter Syndrome / physiopathology
  • Male
  • Retrospective Studies