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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Detalles Bibliográficos
Autores principales: Akira, Maiko, Suzuki, Hitoshi, Ikeda, Arisa, Iwasaki, Masako, Honda, Daisuke, Takahara, Hisatsugu, Rinno, Hisaki, Tomita, Shigeki, Suzuki, Yusuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272369/
https://www.ncbi.nlm.nih.gov/pubmed/34246230
http://dx.doi.org/10.1186/s12882-021-02466-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272369/
https://www.ncbi.nlm.nih.gov/pubmed/34246230
http://dx.doi.org/10.1186/s12882-021-02466-z

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