Nephrology · Nephrology / Hereditary kidney disease
Pierson syndrome
also: Microcoria–congenital nephrosis syndrome
Congenital nephrotic syndrome with ocular abnormalities.
- Specialty
- Nephrology
- Subspecialty
- Nephrology / Hereditary kidney disease
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, neonatal
- Gene(s) involved
- LAMB2
- Alternative names & eponyms
- Microcoria–congenital nephrosis syndrome
Etiology & mechanism
LAMB2 variants affect glomerular basement membrane.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Pierson 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
Allan–Herndon–Dudley syndrome
hypotonia
1 shared
Benign hereditary chorea
hypotonia
1 shared
Brain–lung–thyroid syndrome
hypotonia
1 shared
Cerebral folate deficiency syndrome
hypotonia
1 shared
Coffin–Siris syndrome
hypotonia
1 shared
Cohen syndrome
hypotonia
1 shared
Congenital myasthenic syndrome
hypotonia
1 shared
Cri du chat syndrome
hypotonia
1 shared
Crigler–Najjar syndrome
hypotonia
1 shared
Down syndrome
hypotonia
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