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Anais Brasileiros de Dermatologia, ISSN 0365-0596, 03/2016, Volume 91, Issue 2, pp. 245 - 247
Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification,... 
Neurofibromatosis | Segmentar neurofibromatosis | Neurofibroma | Skin Neoplasms - pathology | Humans | Adult | Male | Rare Diseases | Neurofibromatoses - pathology | Skin - pathology | Syndrome | segmentar neurofibromatosis | Syndrome in Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 11/2015, Volume 90, Issue 6, pp. 909 - 911
Morbihan Syndrome is a rare entity with unknown etiology. It is clinically characterized by chronic erythematous edema on the face - especially in the middle... 
Erythema | Face | Edema | DERMATOLOGY | Blepharitis - pathology | Erythema - pathology | Humans | Adult | Male | Facial Dermatoses - pathology | Chronic Disease | Edema - pathology | Syndrome | Syndrome in Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 05/2016, Volume 91, Issue 3, pp. 387 - 389
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 07/2015, Volume 90, Issue 3, pp. 423 - 425
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 07/2015, Volume 90, Issue 4, pp. 589 - 590
Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmentation changes and minor facial malformations. It has four... 
Inborn | Genetic | Deafness | Skin diseases | Genetic diseases | Waardenburg syndrome | Waardenburg Syndrome - physiopathology | Phenotype | Waardenburg Syndrome - diagnosis | Humans | Deafness - physiopathology | Female | Child | Early Diagnosis | Deafness - diagnosis | Genetic diseases, inborn | Skin diseases, genetic | Syndrome in Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2015, Volume 90, Issue 2, pp. 270 - 271
Immunoglobulin light chain amyloidosis is the most common acquired systemic amyloidosis. Its presentation is often insidious and progressive, which may delay... 
Amyloidosis | diffuse | Skin manifestations | Scleroderma | DERMATOLOGY | Scleroderma, diffuse | Syndrome in Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2015, Volume 90, Issue 1, pp. 131 - 133
The authors describe a case of Cowden's syndrome in a female patient with classic cutaneous lesions, plus papillomatous lesions in the gastrointestinal tract... 
Multiple hamartoma syndrome | Papilloma | Hamartoma | Multiple Hamartoma Syndrome | DERMATOLOGY | Syndrome in Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2014, Volume 89, Issue 2, pp. 363 - 364
Hay-Wells syndrome or AEC (Ankyloblepharon, Ectodermal dysplasia and Cleft lip and palate syndrome) is a rare ectodermal disorder. The treatment is aimed to... 
Skin diseases, genetic | Cleft palate | ANKYLOBLEPHARON | MUTATION | P63 | Ectodermal dysplasia | DERMATOLOGY | Syndrome in Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 11/2014, Volume 89, Issue 6, pp. 1005 - 1006
Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings... 
Ras | Genes | Costello syndrome | Proto-oncogenes | Genes, ras | Syndrome In Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2014, Volume 89, Issue 5, pp. 843 - 844
Vulvovaginal-gingival syndrome is characterized by erosions and desquamation of the vulva, vagina, and gingiva. We reported a case of a 32-year-old woman... 
Tacrolimus | Lichen planus | Therapeutics | Biopsy | Humans | Adult | Female | Gingivitis - pathology | Keratosis - pathology | Lichen Planus - pathology | Vulvovaginitis - pathology | Syndrome | Syndrome In Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2014, Volume 89, Issue 2, pp. 361 - 362
Multiple autoimmune syndrome is a rare condition, described by Humbert and Dupond in 1988. It is defined by the association of at least 3 autoimmune diseases... 
Psoriasis | DISORDERS | Crohn's disease | Alopecia areata | DERMATOLOGY | Vitiligo | Alopecia | Lichen planus, oral | DISEASE | PATIENT | Autoimmune diseases | MULTIPLE AUTOIMMUNE SYNDROME | OF-THE-LITERATURE | oral | Lichen planus | Syndrome in Question
Journal Article
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2014, Volume 89, Issue 1, pp. 177 - 179
The authors present a male 40-year-old patient with established diagnosis of Behcet's disease which had evolved to recurrent bilateral auricular polychondritis... 
Behcet syndrome | Aphthous | Stomatitis | Polychondritis | Vasculitis | Relapsing | relapsing | RELAPSING POLYCHONDRITIS | MAGIC SYNDROME | MOUTH | Behcet Syndrome | GENITAL ULCERS | BEHCETS-DISEASE | INFLAMED CARTILAGE | DERMATOLOGY | aphthous | Polychondritis, relapsing | Stomatitis, aphthous | Syndrome In Question
Journal Article
Journal Article
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, ISSN 1434-6621, 04/2016, Volume 54, Issue 4, pp. E143 - E144
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2014, Volume 89, Issue 1, pp. 175 - 176
Brooke-Spiegler syndrome is an autosomal dominant disorder with variable penetrance and expression. It is characterized by a genetic predisposition to develop... 
Skin diseases, genetic | Neoplasms, adnexal and skin appendage | Skin neoplasms | genetic | Skin diseases | Neoplasms | BROOKE-SPIEGLER-SYNDROME | adnexal and skin appendage | DERMATOLOGY | Syndrome In Question
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 07/2016, Volume 91, Issue 4, pp. 541 - 543
Journal Article
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