49,XXXXX syndrome

From WikiMD's free health, diet & wellness encyclopedia
Jump to navigation Jump to search

Alternate names

Pentasomy X; Chromosome XXXXX syndrome; Penta-X syndrome; Pentasomy X syndrome; Chromosome X pentasomy


Pentasomy X is a sex chromosome anomaly caused by the presence of three extra X chromosomes in females (49,XXXXX instead of 46,XX).

Foetal karyotype demonstrating pentasomy X.png


The prevalence is unknown but less than 40 cases have been described in the literature so far.


  • Pentasomy X is generally thought to arise as a result of successive maternal nondisjunction during meiosis.
  • The features of the syndrome likely arise due to failure of X-inactivation and the presence of multiple X chromosomes from the same parent causing problems with parental imprinting.
  • In theory, X-inactivation should occur and leave only one X chromosome active in each cell. However, failure of this process has been observed in one individual studied.
  • The reason for this is thought to be the presence of an unusually large, and imbalanced, number of X chromosomes interfering with the process.

Signs and symptoms

Clinical presentation

For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed.

80%-99% of people have these symptoms

  • Low-set, posteriorly rotated ears
  • Muscular hypotonia(Low or weak muscle tone)

30%-79% of people have these symptoms

  • Camptodactyly of finger(Permanent flexion of the finger)
  • Clinodactyly of the 5th finger(Permanent curving of the pinkie finger)
  • Global developmental delay
  • Hypertelorism(Wide-set eyes)
  • Intellectual disability(Mental deficiency)
  • Microcephaly(Abnormally small skull)
  • Micrognathia(Little lower jaw)
  • Plagiocephaly(Flat head syndrome)
  • Radioulnar synostosis(Fused forearm bones)
  • Short foot(Short feet)
  • Short stature(Decreased body height)
  • Small hand(Disproportionately small hands)
  • Strabismus(Cross-eyed)
  • Upslanted palpebral fissure(Upward slanting of the opening between the eyelids)
  • Wide nasal bridge(Broad nasal bridge)

5%-29% of people have these symptoms


Diagnosis is suspected based on symptoms and confirmed by chromosomal analysis.


Treatment is based on symptoms.

NIH genetic and rare disease info

49,XXXXX syndrome is a rare disease.

Latest research - 49,XXXXX syndrome

Clinical trials


49,XXXXX syndrome is part of WikiMD's free ^articles!

^49,XXXXX syndrome (article) is provided for informational purposes only. No expressed or implied warranties as to the validity of content.
WikiMD is not a substitute for professional advice. By accessing and using WikiMD you agree to the terms of use.
Templates etc. when imported from Wikipedia, are licensed under CC BY-SA 3.0. See full disclaimers.
W8MD weight loss logo

Ad. Tired of being overweight?. W8MD's physician weight loss program can HELP. Tele medicine available