Hematology · Hematology / Vitamin deficiencies
Thiamine-responsive megaloblastic anemia syndrome
also: Rogers syndrome
Megaloblastic anemia, diabetes and sensorineural deafness responsive to thiamine.
- Specialty
- Hematology
- Subspecialty
- Hematology / Vitamin deficiencies
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes
- Gene(s) involved
- SLC19A2
- Alternative names & eponyms
- Rogers syndrome
Etiology & mechanism
Thiamine transporter defect.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Thiamine-responsive megaloblastic anemia 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.
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Shares symptoms with
3 shared
Wolfram syndrome
diabetes mellitus, optic atrophy, sensorineural deafness
2 shared
Brown–Vialetto–Van Laere syndrome
optic atrophy, sensorineural deafness
1 shared
Barakat syndrome
sensorineural deafness
1 shared
Cardio-facio-cutaneous syndrome
cardiac defects
1 shared
Cobalamin C syndrome
megaloblastic anemia
1 shared
EAST syndrome
sensorineural deafness
1 shared
Folate malabsorption syndrome
megaloblastic anemia
1 shared
Foster Kennedy syndrome
optic atrophy
1 shared
Imerslund–Gräsbeck syndrome
megaloblastic anemia
1 shared
KID syndrome
sensorineural deafness
Shares genes with
None.
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