Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report

BACKGROUND: Nephronophthisis (NPHP) is a chronic tubular interstitial disorder that exhibits an autosomal recessive genetic form and causes progressive renal failure in children. Patients with NPHP rarely show urinary abnormalities, edema, or hypertension. Thus, NPHP is often detected only when rena...

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Detalhes bibliográficos
Publicado no:BMC Nephrol
Main Authors: Akira, Maiko, Suzuki, Hitoshi, Ikeda, Arisa, Iwasaki, Masako, Honda, Daisuke, Takahara, Hisatsugu, Rinno, Hisaki, Tomita, Shigeki, Suzuki, Yusuke
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2021
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8272369/
https://ncbi.nlm.nih.gov/pubmed/34246230
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-021-02466-z
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