Face Abnormalities
Mostrando 1-12 de 47 artigos, teses e dissertações.
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1. Darier disease: the use of dermoscopy in monitoring acitretin treatment
Abstract Darier disease is an uncommon autosomal dominant inherited disease, caused by a mutation in the ATP2A2 gene. The clinical findings are hyperkeratotic papules on the trunk, scalp, face, and neck, maceration of intertriginous areas, palmar pits, whitish papules on the oral mucosa and nail abnormalities. The main histopathologic findings are acantholys
Anais Brasileiros de Dermatologia. Publicado em: 2022
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2. Relation of Dental Anomalies with Occlusal Alterations in the Pediatric Patients
Abstract Objective: To identify the dental anomalies that can modify the occlusal characteristics and their distribution in these occlusal alterations in the skeletal patterns of children. Material and Methods: We analyzed charts, panoramic and periapical radiographs of children aged 5 to 12 years from 2009 to 2012. The facial pattern was evaluated through
Pesqui. Bras. Odontopediatria Clín. Integr.. Publicado em: 10/10/2019
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3. Panniculitis in childhood-onset systemic lupus erythematosus: a multicentric cohort study
Abstract Objective: To evaluate prevalence, clinical manifestations, laboratory abnormalities, treatment and outcome in a multicenter cohort of childhood-onset systemic lupus erythematosus (cSLE) patients with and without panniculitis. Methods: Panniculitis was diagnosed due to painful subcutaneous nodules and/or plaques in deep dermis/subcutaneous tissues
Adv. rheumatol.. Publicado em: 29/07/2019
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4. Do you know this syndrome? Schimmelpenning-Feuerstein-Mims syndrome
Abstract Nevus sebaceous is the most common type of organoid epidermal nevus, often located on the face, following the Blaschko's lines and with alterations in the ipsilateral central nervous system. Distinct disorders can be distinguished by the type of association with epidermal nevus. Schimmelpenning-Feuerstein-Mims syndrome is a rare multisystem disorder
An. Bras. Dermatol.. Publicado em: 09/05/2019
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5. PHACE syndrome: clinical manifestations, diagnostic criteria, and management
Abstract: Infantile hemangioma can be linked to other organ malformations. In 1996, PHACE syndrome was first defined as the association of large and segmental infantile hemangioma, usually on the face, head, or cervical region, with malformations of the posterior fossa of the brain, arterial anomalies of the central nervous system, coarctation of the aorta,
An. Bras. Dermatol.. Publicado em: 2018-06
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6. Do you know this syndrome? Werner syndrome
Abstract: Werner syndrome is a rare autosomal recessive disorder, caused by mutations in the WRN gene. Clinical findings include: senile appearance, short stature, grey hair, alopecia, bird-like face, scleroderma-like skin changes, skin ulcers, voice abnormalities, cataracts, osteoporosis, type 2 diabetes mellitus, ischemic heart disease and hypogonadism. Th
An. Bras. Dermatol.. Publicado em: 2017-03
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7. Fragile X syndrome: panoramic radiographic evaluation of dental anomalies, dental mineralization stage, and mandibular angle
ABSTRACT Fragile X syndrome (FXS) is a disorder linked to the chromosome X long arm (Xq27.3), which is identified by a constriction named fragile site. It determines various changes, such as behavioral or emotional problems, learning difficulties, and intellectual disabilities. Craniofacial abnormalities such as elongated and narrow face, prominent forehead,
J. Appl. Oral Sci.. Publicado em: 2016-10
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8. First case of congenital idiopathic hypohidrosis in China
AbstractA 43-year-old Chinese man presented with generalized hypohidrosis, which he had had since birth, without obvious abnormalities of other skin appendages except a sparse beard and axillary hairs. The sweat test revealed localized sweating on the face, axillae and palms. Histopathologic examination showed that the sweat glands were absent in the forearm
An. Bras. Dermatol.. Publicado em: 2015-10
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9. Audiological Findings in Patients with OculoAuriculo-Vertebral Spectrum
Introduction Oculo-auriculo-vertebral spectrum, also referred to as Goldenhar syndrome, is a condition characterized by alterations involving the development of the structures of the first and second branchial arches. The abnormalities primarily affect the face, the eyes, the spine, and the ears, and the auricular abnormalities are ass
Int. Arch. Otorhinolaryngol.. Publicado em: 2015-03
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10. Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma
It has been reported that, compared with simple increased nuchal translucency, fetal cases with septated cystic hygroma (CH) are more likely to face perinatal handicaps. However, pediatric outcomes and proper prenatal counseling for this anomaly have not yet been truly defined. We performed this study to determine pregnancy and pediatric outcomes of fetuses
Braz J Med Biol Res. Publicado em: 25/07/2014
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11. Estética facial e funções orofaciais em indivíduos com deformidade dentofacial / Facial aesthetics and orofacial functions in individuals with dentofacial deformities
A atratividade da face está relacionada diretamente à autoestima e às relações interpessoais, envolvendo diferentes áreas da saúde, como a medicina, a odontologia e também a fonoaudiologia, porém, com critérios diferentes. Tendo em vista que a ação muscular envolvida nas funções orofaciais é dependente da estrutura na qual está inserida, algu
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 26/06/2012
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12. Disgenesias dentárias na síndrome Richieri-Costa-Pereira / Tooth abnormalities in the Richieri-Costa-Pereira syndrome
Objetivo: Investigar a prevalência de disgenesias dentárias em indivíduos com síndrome Richieri-Costa-Pereira. Material e Métodos: 13 indivíduos, registrados no Hospital de Reabilitação de Anomalias Craniofaciais - Universidade de São Paulo (HRAC-USP), Bauru Brasil, com síndrome Richieri-Costa-Pereira, de ambos os gêneros, de etnia branca, acima d
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 05/12/2011