Severe renal magnesium and calcium wasting with progressive renal failure.
- Specialty
- Nephrology
- Subspecialty
- Nephrology / Tubular disorders
- Sex & age distribution
- Male: affected; Female: affected; Children: yes, childhood
- Gene(s) involved
- CLDN16, CLDN19
- Alternative names & eponyms
- FHHNC
Etiology & mechanism
Paracellin-1 (claudin-16) or claudin-19 defect.
Gene(s) involved (2)
Symptoms & signs (6)
In plain terms, someone with Michelis–Castrillo 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
2 shared
Bartter syndrome
nephrocalcinosis, polyuria
1 shared
Amelogenesis imperfecta with nephrocalcinosis syndrome
nephrocalcinosis
1 shared
Ask–Upmark kidney syndrome
urinary tract infection
1 shared
Conn syndrome
polyuria
1 shared
Fanconi syndrome
polyuria
1 shared
Fanconi–Bickel syndrome
polyuria
1 shared
Hinman syndrome
urinary tract infection
1 shared
Hyperparathyroidism–jaw tumor syndrome
kidney stones
1 shared
Kelley–Seegmiller syndrome
kidney stones
1 shared
Lesch–Nyhan syndrome
kidney stones
Shares genes with
None.
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