Jump to content

Mickleson syndrome

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Citation bot (talk | contribs) at 11:22, 3 September 2020 (Alter: journal. | You can use this bot yourself. Report bugs here. | Suggested by Abductive | Category:Rare diseases | via #UCB_Category). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Mickleson syndrome

Mickleson syndrome is a very rare congenital condition that is characterized by intellectual disability and/or facial anomalies. It was first described by K.N. Mickleson in 1983.[1]

References

  1. ^ Mickleson, K. N. (1983). "Developmental delay, cupid's bow of the upper lip, short great toes, and skull abnormalities". Journal of Clinical Dysmorphology. 4 (1): 21–23.