Results 151 to 160 of about 3,504 (191)

Birt-Hogg-Dube syndrome: a case genodermatosis

, 2015
Yavuz, İbrahim Halil, Güneş Bilgili, Serap, DEMIRCAN, YUHANIZE TAS, KARADAG, AS, KÖSEM, MUSTAFA   +4 more
core  

Preliminary observation on dermatoglyphics in genodermatosis.

Indian journal of dermatology, 1970
openaire   +1 more source

Mastocitosis cutánea. Un caso singular

Revista Habanera de Ciencias Médicas
Jorge Luis Valdés González, Urbano Solís Cartas, Elda María Valdés González   +2 more
doaj  

Genodermatosis

, 2008
Alfred T Lane, Joseph G Morelli
exaly   +3 more sources

Kindler syndrome: a focal adhesion genodermatosis

British Journal of Dermatology, 2009
Kindler syndrome (OMIM 173650) is an autosomal recessive genodermatosis characterized by trauma-induced blistering, poikiloderma, skin atrophy, mucosal inflammation and varying degrees of photosensitivity. Although Kindler syndrome is classified as a subtype of epidermolysis bullosa, it has distinct clinicopathological and molecular abnormalities.
S Akdeniz, John A Mcgrath, J E Lai-Cheong   +2 more
exaly   +5 more sources

H syndrome: A rare genodermatosis

Journal of Cosmetic Dermatology, 2020
[Abstract Not Available]
Isa An, Murat ÖZTÜRK, Erhan Ayhan
exaly   +3 more sources

Lipoid proteinosis: A rare genodermatosis with multisystemic manifestations—A case report

Clinical Case Reports (discontinued)
Key Clinical Message Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis, which is characterized by the deposition of amorphous hyaline material in various tissues, including the mucosa, visceral organs, and skin.

exaly   +2 more sources

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Oral Genodermatosis

2021
exaly   +2 more sources