نتایج جستجو برای: holoprosencephaly

تعداد نتایج: 755  

Journal: :Online Journal of Otolaryngology and Rhinology 2020

Journal: :Proceedings of the National Academy of Sciences 2006

Journal: :American Journal of Medical Genetics Part C: Seminars in Medical Genetics 2018

Journal: :AJNR. American journal of neuroradiology 2002
Erin M Simon Robert F Hevner Joseph D Pinter Nancy J Clegg Mauricio Delgado Stephen L Kinsman Jin S Hahn A James Barkovich

BACKGROUND AND PURPOSE The middle interhemispheric variant of holoprosencephaly (MIH) is a rare malformation in which the cerebral hemispheres fail to divide in the posterior frontal and parietal regions. We herein describe the structural abnormalities of the brain in a large group of patients with MIH, compare these features with those of classic holoprosencephaly (HPE), and propose a developm...

2014
Sanae Abakka Mounia Yousfi

A 30 year old woman, gravida 3 para 2, was admitted to the labour ward at term. Routine ultrasound scan performed at 23 weeks had revealed a single cerebral ventricle, fused thalami and absent midline structures (Panel A), with anti-CMV IgG increasing from 250 to 539 IU/mL at 23 and 25 weeks. Antenatal diagnosis of alobar holoprosencephaly following congenital CMV infection was made. The partur...

Journal: :Journal of medical genetics 1997
C P Chen S L Shih F F Liu S W Jan

Cebocephaly and sirenomelia are uncommon birth defects. Their association is extremely rare; however, the presence of spina bifida with both conditions is not unexpected. We report on a female still-birth with cebocephaly, alobar holoprosencephaly, cleft palate, lumbar spina bifida, sirenomelia, a single umbilical artery, and a 46,XX karyotype, but without maternal diabetes mellitus. Our case a...

Journal: :Medical ultrasonography 2015
Edward Araujo Júnior Liliam Cristine Rolo Gabriele Tonni Sina Haeri Rodrigo Ruano

We present our experience in the contribution of three-dimensional ultrasonography, using the rendering mode, to the prenatal diagnosis of congenital anomalies including neurological defects (acrania/anencephaly, encephalocele, holoprosencephaly), facial anomalies (cyclopia and facial clefts), abdominal wall defects (omphalocele and gastroschisis) and defects of extremities (fetal muscle-skelet...

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