Cover Image

Hyalinosis cutis et mucosae and Ehlers-Danlos syndrome: a rare combination of syndromes

We report on a 7-year-old boy suffering from two rare genetic diseases, namely hyalinosis cutis et mucosae and Ehlers-Danlos syndrome. The diagnosis was finally established after 7 years, by means of light and electron microscopy and immunohistology. Therefore, this report deals with the typical cli...

Full description

Saved in:
Bibliographic Details
Main Authors: König, Insa (Author) , Haußer-Siller, Ingrid (Author) , Anton-Lamprecht, Ingrun (Author) , Schroeter, Renate (Author) , Petzoldt, Detlef (Author)
Format: Article (Journal)
Language:English
Published: 1994
In: Der Hautarzt
Year: 1994, Volume: 45, Issue: 2, Pages: 108-112
ISSN:1432-1173
DOI:10.1007/s001050050049
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s001050050049
Get full text
Author Notes:Insa König, Ingrid Haußer, Ingrun Anton-Lamprecht, Renate Schröter, Detlef Petzoldt
Description
Summary:We report on a 7-year-old boy suffering from two rare genetic diseases, namely hyalinosis cutis et mucosae and Ehlers-Danlos syndrome. The diagnosis was finally established after 7 years, by means of light and electron microscopy and immunohistology. Therefore, this report deals with the typical clinical and morphological features of both genetic disorders.
Item Description:Gesehen am 04.10.2023
Physical Description:Online Resource
ISSN:1432-1173
DOI:10.1007/s001050050049

Similar Items