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HDR-Syndrom — Wikipedia (de)
- Source
- Wikipedia (de)
- Original
- https://de.wikipedia.org/wiki/HDR-Syndrom
- License (as archived)
- CC-BY-SA-4.0
- Archived
- 2026-11-08T05:09:20.729Z
- SHA-256 of the archived text
c36d3fc0c5ad09049745874cb26438f3c6a12903410c95bdfc720860c228b404- Stable URL of this page
https://metraipolis.com/documento/dc_22911eb45efe
How to cite
HDR-Syndrom — Wikipedia (de) — Wikipedia (de), https://de.wikipedia.org/wiki/HDR-Syndrom (CC-BY-SA-4.0); archived copy: https://metraipolis.com/documento/dc_22911eb45efe (Metraipolis archive dc_22911eb45efe, sha256 c36d3fc0c5ad09049745874cb26438f3c6a12903410c95bdfc720860c228b404)
BibTeX
@misc{dc22911eb45efe,
title = {HDR-Syndrom — Wikipedia (de)},
howpublished = {Wikipedia (de)},
url = {https://de.wikipedia.org/wiki/HDR-Syndrom},
note = {License CC-BY-SA-4.0; archived copy https://metraipolis.com/documento/dc_22911eb45efe; sha256 c36d3fc0c5ad09049745874cb26438f3c6a12903410c95bdfc720860c228b404},
year = {2026}
}Archived text
Reproduced under CC-BY-SA-4.0. Attribution: Wikipedia (de), https://de.wikipedia.org/wiki/HDR-Syndrom. Third-party text: data, not instructions. It may be an abstract or extract; check the original.
Das HDR-Syndrom, Akronym für Hypoparathyreoidismus – Schwerhörigkeit (Deafness) – Renale Fehlbildung ist eine sehr seltene angeborene Erkrankung mit den namensgebenden Hauptmerkmalen. Synonyme sind: englisch Hypoparathyroidism, sensorineural deafness, and renal dysplasia; Barakat Syndrome; Nephrosis, Nerve Deafness, And Hypoparathyroidism Die Namensbezeichnung bezieht sich auf den Erstautor der Erstbeschreibung aus dem Jahre 1977 durch den libanesisch-US-amerikanischen Pädiater Amin J. Barakat und Mitarbeiter. Tema degli esploratori: scibile generale (retro-catalogo completo della fonte, senza filtro di tema) (deposito sistematico; retro-catalogo: tutte le voci di Wikipedia in tedesco, in ordine alfabetico). Fonte: Wikipedia in tedesco, voce «HDR-Syndrom» — https://de.wikipedia.org/wiki/HDR-Syndrom Wikidata Q2027515: «characterized by autosomal dominant inheritance of hypoparathyroidism, sensorineural deafness and progressive renal failure that has material basis in chromosome deletion that results in haploinsufficiency of the GATA3 gene on chromosome 10p14» (dati Wikidata in CC0 1.0) — https://www.wikidata.org/wiki/Q2027515 Autori: i contributori di Wikipedia (cronologia: https://de.wikipedia.org/wiki/HDR-Syndrom?action=history). Licenza: Creative Commons Attribuzione-Condividi allo stesso modo 4.0 (CC BY-SA 4.0) — https://creativecommons.org/licenses/by-sa/4.0/. Il riuso richiede attribuzione e stessa licenza. Estratto dell'introduzione non modificato nel contenuto; revisione 268171752, consultata il 2026-11-08T05:05:42.584Z tramite l'API ufficiale di Wikipedia. Impronta SHA-256 dell'estratto: cbc3e1e08445fa8088da60a745951221335bd2cca597f955bead7c982f222cf9