Skip to main content
Erschienen in: Pediatric Nephrology 2/2020

19.08.2019 | Clinical Quiz

A rare cause of chronic hyponatremia in an infant: Answers

verfasst von: Gül Yeşiltepe Mutlu, Mehmet Taşdemir, Nuray Uslu Kızılkan, Tülay Güran, Şükrü Hatun, Hülya Kayserili, Ilmay Bilge

Erschienen in: Pediatric Nephrology | Ausgabe 2/2020

Einloggen, um Zugang zu erhalten

Excerpt

Due to the presence of vomiting and failure to thrive, renal tubular disorders, gastrointestinal disorders, and endocrinologic abnormalities were considered in the differential diagnosis. Failure to thrive, polyuria, mild hyponatremia, and mild hyperkalemia were suggestive of renal tubular disorders, but she had normal serum phosphate and calcium levels, normal blood gases, and no glucosuria or proteinuria. Thus, renal tubular acidosis was ruled out. …
Literatur
3.
Zurück zum Zitat Arai K, Chrousos GP (2000) Aldosterone deficiency and resistance. [Updated 2016 May 11]. In: Feingold KR, Anawalt B, Boyce A, et al (eds) Endotext [Internet]. MDText.com, South Dartmouth Arai K, Chrousos GP (2000) Aldosterone deficiency and resistance. [Updated 2016 May 11]. In: Feingold KR, Anawalt B, Boyce A, et al (eds) Endotext [Internet]. MDText.com, South Dartmouth
6.
Zurück zum Zitat Shohat M (1993) Familial Mediterranean fever. University of Washington, Seattle Shohat M (1993) Familial Mediterranean fever. University of Washington, Seattle
9.
Zurück zum Zitat Wasniewska M, De Luca F, Valenzise M et al (2001) Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene. Eur J Endocrinol 144:59–62CrossRef Wasniewska M, De Luca F, Valenzise M et al (2001) Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene. Eur J Endocrinol 144:59–62CrossRef
11.
Zurück zum Zitat Zhang G, Rodriguez H, Fardella CE et al (1995) Mutation T318M in the CYP11B2 gene encoding P450c11AS (aldosterone synthase) causes corticosterone methyl oxidase II deficiency. Am J Hum Genet 57:1037–1043PubMedPubMedCentral Zhang G, Rodriguez H, Fardella CE et al (1995) Mutation T318M in the CYP11B2 gene encoding P450c11AS (aldosterone synthase) causes corticosterone methyl oxidase II deficiency. Am J Hum Genet 57:1037–1043PubMedPubMedCentral
13.
Zurück zum Zitat Peter M, Bünger K, Drop SL, Sippell WG (1998) Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies. Eur J Endocrinol 139:96–100CrossRef Peter M, Bünger K, Drop SL, Sippell WG (1998) Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies. Eur J Endocrinol 139:96–100CrossRef
Metadaten
Titel
A rare cause of chronic hyponatremia in an infant: Answers
verfasst von
Gül Yeşiltepe Mutlu
Mehmet Taşdemir
Nuray Uslu Kızılkan
Tülay Güran
Şükrü Hatun
Hülya Kayserili
Ilmay Bilge
Publikationsdatum
19.08.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Nephrology / Ausgabe 2/2020
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-019-04337-0

Weitere Artikel der Ausgabe 2/2020

Pediatric Nephrology 2/2020 Zur Ausgabe

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.