Historical evidence for the genetic heterogeneity of pseudoxanthoma elasticum
FM Pope - British Journal of Dermatology, 1975 - Wiley Online Library
Re‐examination of published data from affected families with pseudoxanthoma elasticum
(PXE) described in the literature between 1896 and 1968 supported the concept of clinical …
(PXE) described in the literature between 1896 and 1968 supported the concept of clinical …
[图书][B] Lexikon der Syndrome und Fehlbildungen
R Witkowski, O Prokop, E Ullrich, R Witkowski… - 1999 - Springer
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A case of Hutchinson-Gilford progeria syndrome mimicking scleredema in early infancy
N Erdem, AT Güneş, O Avcı, E Osma - Dermatology, 1994 - karger.com
We report a case of Hutchinson-Gilford progeria syndrome (HGPS). The patient showed the
characteristics of scleredema at the age of 2.5 months but developed all the manifestations …
characteristics of scleredema at the age of 2.5 months but developed all the manifestations …
Premature multiple Bowen's disease in poikiloderma congenitale with warty hyperkeratoses
E Haneke, E Gutschmidt - Dermatology, 1979 - karger.com
Short Communication Premature Multiple Bowen’s Disease in Poikiloderma congenitale
with Warty Hyperkeratoses Page 1 Short Communication Dermatológica 158: 384-388 (1979) …
with Warty Hyperkeratoses Page 1 Short Communication Dermatológica 158: 384-388 (1979) …
Erbliche verhornungsstörungen der Haut
UW Schnyder, W Klunker - Vererbung von Hautkrankheiten, 1966 - Springer
Die erblichen Verhornungsstörungen der Haut werden an dieser Stelle unter dem
Gesichtspunkt der Vererbungsforschung abgehandelt, während die umfassende …
Gesichtspunkt der Vererbungsforschung abgehandelt, während die umfassende …
Fluorescein study of a family with angioid streaks and pseudoxanthoma elasticum.
DS Hull, TM Aaberg - The British Journal of Ophthalmology, 1974 - ncbi.nlm.nih.gov
Method Members of two consecutive generations of a family with known pseudoxanthoma
elasticum were studied by indirect ophthalmoscopy, fundus biomicroscopy, colour fundus …
elasticum were studied by indirect ophthalmoscopy, fundus biomicroscopy, colour fundus …
Vorwiegend cutane Dermatosen
G Achten, E Grosshans, T Hardmeier, K Mach… - Haut und …, 1973 - Springer
Von den Hauterkrankungen unklarer oder unbekannter Ätiologie spielen sich viele
vorwiegend oder ausschließlich in der Cutis ab. Sie lassen sich in folgende fünf Gruppen …
vorwiegend oder ausschließlich in der Cutis ab. Sie lassen sich in folgende fünf Gruppen …
Pseudoxanthoma elasticum—Groenblad-Strandberg-Syndrom—Elastorrhexis systematisata. Eine Literaturanalyse
SB Stutz, W Schmid - Neue Entwicklungen in der Dermatologie: Band 4, 1987 - Springer
Summary In 1974 Pope divided the Pseudoxanthoma elasticum (PXE) into 2 autosomal-
dominant and 2 autosomal-recessive types using clinical and genetical criteria. Although we …
dominant and 2 autosomal-recessive types using clinical and genetical criteria. Although we …
Autosomal und X-chromosomal recessiv vererbte Syndrome mit Hautbeteiligung, welche mit einer erhöhten Tumorincidenz einhergehen
T Šalamon - Neue Entwicklungen in der Dermatologie: Band 5, 1988 - Springer
The clinical symptoms, various laboratory findings, genetics, differential diagnosis,
prognosis and treatment of some autosomal recessively and X-chromosomal recessively …
prognosis and treatment of some autosomal recessively and X-chromosomal recessively …
Pseudoxanthoma Elasticum
A Han, M Lebwohl - Harper's Textbook of Pediatric …, 2011 - Wiley Online Library
Pseudo‐xanthoma elasticum is a rare, inherited disease characterized by progressive
calcification and fragmentation of elastic tissue in the skin, eyes and cardiovascular system …
calcification and fragmentation of elastic tissue in the skin, eyes and cardiovascular system …