Congenital Lymphedema
What's New
Last Posted: May 02, 2023
- Possible biallelic inheritance in TIE1 in a family with congenital lymphedema, intestinal lymphangiectasia and cutis aplasia.
Aasem Abu Shtaya, et al. Clinical genetics 2023 0 - Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome.
Boone Philip M, et al. American journal of medical genetics. Part A 2019 0 (1) 189-194 - Heterozygous deletion of the VEGFC gene in 4q34.3 is associated with Milroy-like lymphedema: First prenatal case report.
Huynh Minh-Tuan, et al. American journal of medical genetics. Part A 2022 0 (12) 3550-3554 - Congenital lymphedema
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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