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LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA

Known as: EMBERGER SYNDROME 
National Institutes of Health

Related topics

Related topics

7 relations
Autosomal dominant inheritanceLeukemia, Myelocytic, AcuteLymphedemaLymphedema (lower extremities)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
[Congenital deaf-mutism with pale complexion and anemia for 1 year in a school-aged girl].
An 11-year-old girl was found to have pale complexion and anemia with gradual aggravation for one year. She was weak in the past… 
2018
2018
Emberger syndrome: A rare association with hearing loss.
2015
2015
First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation
To the Editor, Emberger syndrome is characterized by congenital deafness and primary lymphedema of the lower limbs, and is… 
2006
2006
In memoriam Prof. Ing. Dr. Vlado Tregubov
Am 8. Januar 1974 ist Prof. Ing. Dr. Vlado Tregubov wfihrend intensiver wissenschaftlicher Arbeit in Ljubljana einem Herzschlag… 
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