Hereditary ectodermal dysplasia and Lyon hypothesis

Introduction: ectodermal dysplasia refers to disorders that promote dysplasia or aplasia structures and tissues derived from ectoderm. This condition is usually inherited by recessive pattern with lincagem cross, taking their frequency and severity more pronounced in men. Objective: the aim was to r...

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Main Authors: Camila Helena Machado da Costa (Author), Maria Luiza dos Anjos Pontual (Author), Andréa dos Anjos Pontual (Author), Ricardo Villar Beltrão (Author), Manuella Santos Carneiro Almeida (Author), Michele Baffi Diniz (Author)
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Published: Editorial Ciencias Médicas, 2015-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Camila Helena Machado da Costa  |e author 
700 1 0 |a Maria Luiza dos Anjos Pontual  |e author 
700 1 0 |a Andréa dos Anjos Pontual  |e author 
700 1 0 |a Ricardo Villar Beltrão  |e author 
700 1 0 |a Manuella Santos Carneiro Almeida  |e author 
700 1 0 |a Michele Baffi Diniz  |e author 
245 0 0 |a Hereditary ectodermal dysplasia and Lyon hypothesis 
260 |b Editorial Ciencias Médicas,   |c 2015-01-01T00:00:00Z. 
500 |a 0034-7507 
500 |a 1561-297X 
520 |a Introduction: ectodermal dysplasia refers to disorders that promote dysplasia or aplasia structures and tissues derived from ectoderm. This condition is usually inherited by recessive pattern with lincagem cross, taking their frequency and severity more pronounced in men. Objective: the aim was to report a case of Hereditary Ectodermal Dysplasia. Case report: patient TVLV female, aged 25, leucoderma, which sought a private radiology service in the city of João Pessoa, Paraíba, Brazil. It was reported by the patient, his father, now deceased, was diagnosed with this syndrome. During the extraoral examination, there was dryness of the lips and eyes, skin darkening in the periocular region, hair thin and sparse. The patient did not reveal xerostomia or episodes of hyperthermia. There was loss of vertical dimension, prominent forehead and nails were normal. The clinical examination intrabucal, there was retention of 11 primary teeth and the absence of 19 permanent teeth. The partial oligodontia was then confirmed by radiographic examination. The partial expression of syndromic features can be explained by the Lyon hypothesis (X inactivation), with half of the X chromosomes of patients expressing normal genes and half the abnormal gene. Conclusions: it was recommended genetic counseling and regular visits to the dentist. It´s fundamental the diagnosis of this disorder for the odontologist even in the cases of softening of signs and symptoms. 
546 |a EN 
546 |a ES 
690 |a displasia ectodérmica 
690 |a anodoncia 
690 |a genética. 
690 |a Dentistry 
690 |a RK1-715 
690 |a Medicine (General) 
690 |a R5-920 
655 7 |a article  |2 local 
786 0 |n Revista Cubana de Estomatología, Vol 52, Iss 1, Pp 58-62 (2015) 
787 0 |n http://www.revestomatologia.sld.cu/index.php/est/article/view/323 
787 0 |n https://doaj.org/toc/0034-7507 
787 0 |n https://doaj.org/toc/1561-297X 
856 4 1 |u https://doaj.org/article/fa6ff79d097e4cb0be9f4b0cd6dc2f25  |z Connect to this object online.