Nephrology · Nephrology / Hereditary kidney disease
Galloway–Mowat syndrome
also: Microcephaly with nephrotic syndrome
Microcephaly, brain malformation and steroid-resistant nephrotic syndrome.
- Specialty
- Nephrology
- Subspecialty
- Nephrology / Hereditary kidney disease
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes
- Gene(s) involved
- GON7, LAGE3, NUP107, NUP133, NUP85, NUP93, OSGEP, TP53RK, TPRKB, WDR4, WDR73
- Alternative names & eponyms
- Microcephaly with nephrotic syndrome
Etiology & mechanism
KEOPS complex and other gene defects.
Gene(s) involved (11)
Symptoms & signs (6)
In plain terms, someone with Galloway–Mowat 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
Angelman syndrome
microcephaly, seizures
2 shared
Cerebral folate deficiency syndrome
microcephaly, seizures
2 shared
Cockayne syndrome
developmental delay, microcephaly
2 shared
Congenital Zika syndrome
microcephaly, seizures
2 shared
Fetal hydantoin syndrome
developmental delay, microcephaly
2 shared
Folate malabsorption syndrome
developmental delay, seizures
2 shared
Glucose transporter type 1 deficiency syndrome
developmental delay, microcephaly
2 shared
Hoyeraal–Hreidarsson syndrome
developmental delay, microcephaly
2 shared
Hyperinsulinism–hyperammonemia syndrome
developmental delay, seizures
2 shared
NARP syndrome
developmental delay, seizures
Shares genes with
None.
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