ISOLATED HEMIHYPERTROPHY IN CHILD

Hemihypertrophy or hemihyperplasia is a rare congenital condition, whose incidence is difficult to estimate, due to the fact that asymmetry is very mild, therefore remaining undiagnosed. Hemihyperplasia can be isolated or associated to certain genetic syndromes. We present the case of a 6-months-old...

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Principais autores: Lorena Elena Melit (Autor), Cristina Oana Marginean (Autor), Claudia Banescu (Autor), Raluca Damian (Autor), Andreea Dinca (Autor), Claudiu Marginean (Autor)
Formato: Livro
Publicado em: Amaltea Medical Publishing House, 2016-12-01T00:00:00Z.
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MARC

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042 |a dc 
100 1 0 |a Lorena Elena Melit  |e author 
700 1 0 |a Cristina Oana Marginean  |e author 
700 1 0 |a Claudia Banescu  |e author 
700 1 0 |a Raluca Damian  |e author 
700 1 0 |a Andreea Dinca  |e author 
700 1 0 |a Claudiu Marginean  |e author 
245 0 0 |a ISOLATED HEMIHYPERTROPHY IN CHILD 
260 |b Amaltea Medical Publishing House,   |c 2016-12-01T00:00:00Z. 
500 |a 10.37897/RJP.2016.4.11 
500 |a 1454-0398 
500 |a 2069-6175 
520 |a Hemihypertrophy or hemihyperplasia is a rare congenital condition, whose incidence is difficult to estimate, due to the fact that asymmetry is very mild, therefore remaining undiagnosed. Hemihyperplasia can be isolated or associated to certain genetic syndromes. We present the case of a 6-months-old female infant, in whom, during the neonatal period, was raised the suspicion of a congenital hemihypertrophy. She was admitted in our clinic due to the presence of a facial asymmetry. The clinical exam revealed also, besides the hemihyperplasia of the right hemiface more obvious at the level of the forehead, a hypertrophy of the right superior and inferior limbs. The laboratory tests identified a mild anemia, increased levels of transaminases and alfa-fetoprotein. The abdominal ultrasound revealed a mild hepatomegaly and the transfontanellar one discrete ventriculomegaly and frontal atrophy. The genetic test was negative, therefore the final diagnosis was of isolated hemihypertrophy. The further re-evaluations showed a decreasing level of alfa-fetoprotein, without other additional pathological elements. The particularity of the case consists in diagnosing an isolated hemohypertrophy in a 6-month-old female infant, with negative genetic test, in whom it was observed at the moment of birth a mild facial asymmetry, with afterwards favorable evolution, with progressive decrease of the alfa-fetoprotein level and normal abdominal ultrasound. 
546 |a EN 
690 |a isolated hemihypertrophy 
690 |a isolated hemihyperplasia 
690 |a infant 
690 |a alfa-fetoprotein 
690 |a Medicine 
690 |a R 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Romanian Journal of Pediatrics, Vol 65, Iss 4, Pp 386-389 (2016) 
787 0 |n https://revistemedicale.amaltea.ro/Romanian_Journal_of_PEDIATRICS/Revista_Romana_de_PEDIATRIE-2016-Nr.4/RJP_2016_4_EN_Art-11.pdf 
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787 0 |n https://doaj.org/toc/2069-6175 
856 4 1 |u https://doaj.org/article/1c009c08c6f841f7ad3231a1ea1ad2ac  |z Connect to this object online.