Hematology · Hematology / Hemoglobinopathies
Hydrops fetalis syndrome
also: Hb Bart's hydrops fetalis syndrome
Severe alpha thalassemia causing fetal hydrops.
- Specialty
- Hematology
- Subspecialty
- Hematology / Hemoglobinopathies
- Sex & age distribution
- Male: affected; Female: affected; Children: yes, prenatal
- Gene(s) involved
- HBA1, HBA2
- Alternative names & eponyms
- Hb Bart's hydrops fetalis syndrome
Etiology & mechanism
Deletion of all four alpha globin genes.
Gene(s) involved (2)
Symptoms & signs (4)
In plain terms, someone with Hydrops fetalis syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
1 shared
Familial chylomicronemia syndrome
hepatosplenomegaly
1 shared
Hunter syndrome
hepatosplenomegaly
1 shared
Hurler syndrome
hepatosplenomegaly
1 shared
Macrophage activation syndrome
hepatosplenomegaly
1 shared
Maroteaux–Lamy syndrome
hepatosplenomegaly
1 shared
Mirror syndrome
fetal hydrops
1 shared
Mucopolysaccharidosis type II with neurological involvement
hepatosplenomegaly
1 shared
Omenn syndrome
hepatosplenomegaly
1 shared
Sly syndrome
hepatosplenomegaly
1 shared
TORCH syndrome
hepatosplenomegaly
Shares genes with
None.
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