Revesz syndrome revisited

Revesz syndrome (RS) is an extremely rare variant of dyskeratosis congenita (DKC) with only anecdotal reports in the literature.

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Bibliographic Details
Main Authors:	Karremann, Michael (Author) , Neumaier-Probst, Eva (Author) , Schlichtenbrede, Frank (Author) , Beier, Fabian (Author) , Brümmendorf, Tim Henrik (Author) , Cremer, Friedrich Walter (Author) , Bader, Peter (Author) , Dürken, Matthias (Author)
Format:	Article (Journal)
Language:	English
Published:	23 October 2020
In:	Orphanet journal of rare diseases Year: 2020, Volume: 15, Pages: 1-13
ISSN:	1750-1172
DOI:	10.1186/s13023-020-01553-y
Online Access:	Verlag, kostenfrei, Volltext: https://doi.org/10.1186/s13023-020-01553-y
Author Notes:	Michael Karremann, Eva Neumaier-Probst, Frank Schlichtenbrede, Fabian Beier, Tim H. Brümmendorf, Friedrich W. Cremer, Peter Bader and Matthias Dürken

Description
Summary:	Revesz syndrome (RS) is an extremely rare variant of dyskeratosis congenita (DKC) with only anecdotal reports in the literature.
Item Description:	Gesehen am 09.12.2021
Physical Description:	Online Resource
ISSN:	1750-1172
DOI:	10.1186/s13023-020-01553-y