Blau syndrome: A new kindred - 29/08/11
Doi : 10.1067/S0190-9622(02)61772-4
Delilah Alonso, MD a, George W Elgart, MD a, Lawrence A Schachner, MD a, ⁎ 
a Department of Dermatology and Cutaneous Surgery, University of Miami School of Medicine., Miami, Florida, USA
*Reprint requests: Lawrence A. Schachner, MD, Department of Dermatology and Cutaneous Surgery, University of Miami School of Medicine, 1600 NW 10th Ave, Room 2023A, R(250), Miami, FL 33136, USA.
Abstract |
Blau syndrome is a rare condition typically defined by granulomatous arthritis, skin eruption, and uveitis occurring in the absence of lung or other visceral involvement. Other characteristic physical findings include synovial cysts and camptodactyly. We describe a new kindred demonstrating autosomal dominant inheritance and anticipation.
Il testo completo di questo articolo è disponibile in PDF.Mappa
© 2003
American Academy of Dermatology, Inc.. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
Vol 49 - N° 2
P. 299-302 - agosto 2003 Ritorno al numero
Articolo precedente
- Fatal interstitial pulmonary fibrosis in anti-Jo-1–negative amyopathic dermatomyositis
- Whitney A High, Jack B Cohen, Bettina A Murphy, Melissa I Costner
- A case of chronic herpes gestationis: Persistent disease or conversion to bullous pemphigoid?
- Lauretta Amato, Sandra Mei, Isabella Gallerani, Silvia Moretti, Paolo Fabbri
Benvenuto su EM|consulte, il riferimento dei professionisti della salute.
L'accesso al testo integrale di questo articolo richiede un abbonamento.
Già abbonato a @@106933@@ rivista ?