Gastroenterology · Gastroenterology / Hepatology
Lucey–Driscoll syndrome
also: Transient familial neonatal hyperbilirubinemia
Transient severe neonatal jaundice from a maternal serum inhibitor.
- Specialty
- Gastroenterology
- Subspecialty
- Gastroenterology / Hepatology
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, neonatal
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Transient familial neonatal hyperbilirubinemia
Etiology & mechanism
Inhibition of UGT1A1 by circulating maternal steroids.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (4)
In plain terms, someone with Lucey–Driscoll 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
2 shared
Crigler–Najjar syndrome
kernicterus, neonatal jaundice
1 shared
Anomalous left coronary artery from pulmonary artery
poor feeding
1 shared
Blue baby syndrome
lethargy
1 shared
Cyclic vomiting syndrome
lethargy
1 shared
Food protein-induced enterocolitis syndrome
lethargy
1 shared
Heterotaxy syndrome
poor feeding
1 shared
Hypoplastic left heart syndrome
poor feeding
1 shared
Kernicterus syndrome
lethargy
1 shared
Neonatal abstinence syndrome
poor feeding
1 shared
Prader–Willi syndrome
poor feeding
Shares genes with
None.
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