Natural history of alpha-thalassemia X-linked intellectual disability syndrome: A case report of a 45-year-old man




Arvio Maria, Lähdetie Jaana

PublisherWILEY

2021

American Journal of Medical Genetics Part A

AMERICAN JOURNAL OF MEDICAL GENETICS PART A

AM J MED GENET A

4

1552-4825

DOIhttps://doi.org/10.1002/ajmg.a.62213

https://doi.org/10.1002/ajmg.a.62213

https://research.utu.fi/converis/portal/detail/Publication/58238935



We have followed the clinical course of a 45-year-old man with a severe form of alpha-thalassemia X-linked intellectual disability syndrome for 40 years. The most challenging health issue is the combination of rumination, drooling, and vomiting. The patient achieved present adaptive and motor skills in his teenage years. He is able to move on the floor in a sitting position. He seems happy and has not shown any behavioral or psychiatric symptoms. New signs not described in the literature before are accelerated growth after puberty and atypical sleeping position with upper body resting on legs.

Last updated on 2024-26-11 at 18:25