Aplasia Cutis Congenita
Mostrando 1-8 de 8 artigos, teses e dissertações.
-
1. Oculoectodermal syndrome: twentieth described case with new manifestations
Abstract Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features of the syndrome: aplasia cutis congenita and epibulbar dermoids. Ou
An. Bras. Dermatol.. Publicado em: 2016-10
-
2. Aplasia cutis congenita of the scalp- what are the steps to be followed? Case report and review of the literature
Aplasia cutis congenita is a rare malformation characterized by localized congenital absence of the skin. It rarely occurs on the trunk and limbs, and can occur in isolation or as part of a heterogeneous group of syndromes. We report a case of a 4-day-old boy with a 5.6-cm- diameter tumor, with a central crust, no
An. Bras. Dermatol.. Publicado em: 2015-02
-
3. Você conhece esta síndrome?
A síndrome de Bart é caracterizada pela tríade de manifestações clínicas: epidermólise bolhosa, aplasia de cútis e anormalidades ungueais. Presume-se que a ausência congênita de pele segue as linhas de Blaschko. O tratamento visa a evitar infecções secundárias. O prognóstico é bom e depende da cicatrização das bolhas.
Anais Brasileiros de Dermatologia. Publicado em: 2010-02
-
4. Aplasia cutis congênita do escalpo
Arquivos de Neuro-Psiquiatria. Publicado em: 2008
-
5. Extensa falha cutânea e craniana em paciente com aplasia cutis congenita
Aplasia cutis congenita (ACC) é doença rara, caracterizada pela ausência de formação completa da pele. Geralmente ocorre no couro cabeludo, na linha mediana, e apresenta-se ao nascimento como uma ferida ulcerada que pode atingir diferentes profundidades e envolver o periósteo, crânio e dura-máter. Descrevemos o caso de menina recem-nascida que aprese
Arquivos de Neuro-Psiquiatria. Publicado em: 2004-12
-
6. Epidermal naevi and bullous aplasia cutis congenita in a neonate.
The case of a neonate with cutaneous lesions consistent with epidermal naevi is presented. In addition to typical epidermal naevi, this baby had an unusual, bullous form of aplasia cutis congenita. Although aplasia cutis has been described as bullous and has been found in association with the epidermal naevus syndrome, both of these occurrences are rare in m
-
7. Extensive form of aplasia cutis congenita: a new syndrome?
Aplasia cutis congenita is a heterogeneous group of conditions usually involving the scalp as well as any other part of the body and is associated with a number of other congenital anomalies. We report on a newborn male with almost complete absence of skin and subcutaneous tissue in association with choanal atresia, syndactyly, imperforate anus, pulmonary hy
-
8. Recessive aplasia cutis congenita of the limbs.
Six inbred persons (five males and one female) in three generations of a single family are reported as having simple congenital absence of skin on the upper or lower limbs or both. The data suggest an autosomal recessive pattern of inheritance for this apparently new clinical entity.