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LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA
Known as:
EMBERGER SYNDROME
National Institutes of Health
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Related topics
Related topics
7 relations
Autosomal dominant inheritance
Leukemia, Myelocytic, Acute
Lymphedema
Lymphedema (lower extremities)
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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].
Ling Chen
,
Xiangling He
,
Keke Chen
Zhongguo dang dai er ke za zhi = Chinese journal…
2019
Corpus ID: 208227381
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…
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2018
2018
Emberger syndrome: A rare association with hearing loss.
F. Zawawi
,
M. Sokolov
,
T. Mawby
,
K. Gordon
,
B. Papsin
,
S. Cushing
International Journal of Pediatric…
2018
Corpus ID: 4560321
2015
2015
First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation
S. Seo
,
Kyu Yeun Kim
,
+4 authors
J. Moon
The Korean Journal of Internal Medicine
2015
Corpus ID: 2900291
To the Editor, Emberger syndrome is characterized by congenital deafness and primary lymphedema of the lower limbs, and is…
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2006
2006
In memoriam Prof. Ing. Dr. Vlado Tregubov
A. Tregubov
,
Vlado Tregubov
Vegetatio
2006
Corpus ID: 27192753
Am 8. Januar 1974 ist Prof. Ing. Dr. Vlado Tregubov wfihrend intensiver wissenschaftlicher Arbeit in Ljubljana einem Herzschlag…
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