Asplenia with right isomerism and complex heart disease.
- Specialty
- Cardiology
- Subspecialty
- Cardiology / Congenital heart disease
- Sex & age distribution
- Male: affected, more common; Female: affected; Children: yes, neonatal
- Gene(s) involved
- ACVR2B, CFC1, NODAL, ZIC3
- Alternative names & eponyms
- Asplenia syndrome
Etiology & mechanism
Laterality gene defects.
Gene(s) involved (4)
Symptoms & signs (6)
In plain terms, someone with Ivemark 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
4 shared
Heterotaxy syndrome
asplenia, cyanosis, howell–jolly bodies, intestinal malrotation
1 shared
Blue baby syndrome
cyanosis
1 shared
Central alveolar hypoventilation syndrome
cyanosis
1 shared
Ectopic ACTH syndrome
infections
1 shared
Eisenmenger syndrome
cyanosis
1 shared
Hepatopulmonary syndrome
cyanosis
1 shared
Immunodysregulation polyendocrinopathy enteropathy X-linked syndrome
infections
1 shared
Infant respiratory distress syndrome
cyanosis
1 shared
Meconium aspiration syndrome
cyanosis
1 shared
Myelodysplastic syndrome
infections
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