Results 101 to 110 of about 11,012 (235)
Middle interhemispheric holoprosencephaly with subdural hematoma
Journal of the Belgian Society of Radiology, 2011 Background: A 4-month-old boy with prenatal sonography findings consistent with corpus callosum agenesis and ventriculomegaly presented. Patient was born at 37-weeks from 18-yearold woman, gravida 1 para 1.
A K Poyraz, M R Onur
doaj +1 more source
Alobar holoprosencephaly associated with a rare chromosomal abnormality
Medicine, 2018 Rationale: Holoprosencephaly is a structural malformation of the brain that results from the complete or incomplete noncleavage of the forebrain of the embryo into 2 hemispheres.
C. Ionescu +6 more
semanticscholar +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Early recognition of syndromic features by dental professionals can lead to timely diagnosis and intervention, especially when systemic anomalies have been overlooked. Preventive and individualized dental management, supported by behavioral guidance, can achieve long‐term stability even in medically complex patients, including those with ...
Nazanin Nasr +4 more
wiley +1 more source
Holoprosencephaly in Texas, 1999 - 2009: A prevalence study
, 2016 This study describes the birth prevalence of the birth defect holoprosencephaly among infants born in Texas between 1999 and 2009. Factors associated with the birth prevalence of holoprosencephaly were also examined using multiple Poisson regression ...
Cartus, Abigail
core +1 more source
Genetics in Medicine, 2017 PurposeWith improved medical care, some individuals with holoprosencephaly (HPE) are surviving into adulthood. We investigated the clinical manifestations of adolescents and adults with HPE and explored the underlying molecular causes.MethodsParticipants
K. Weiss +20 more
semanticscholar +1 more source
Causes, Types, and Outcome of Holoprosencephaly
, 2004 Recent advances in genetics and neuroimaging of children with holoprosencephaly (HPE) are reviewed from Stanford University School of Medicine ...
J Gordon Millichap
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Alobar holoprosencephaly, proboscis and cyclopia in a chromosomally normal fetus: Prenatal diagnosis and fetal outcome [PDF]
, 2016 Holoprosencephaly is a brain malformation that develops as a result of a defect in development of prosencephalon during early gestation. Holoprosencephaly can be diagnosed with prenatal ultrasonography and magnetic resonance imaging.
Genç, Mine +4 more
core +1 more source
Pediatric cerebral thrombosis is a lifelong neurodevelopmental condition
Developmental Medicine &Child Neurology, Volume 68, Issue 9, Page 1176-1177, September 2026.
Aleksandra Mineyko
wiley +1 more source
Correlation of Ultrasonography and MRI in Prenatal Diagnosis of Lobar Holoprosencephaly
Gynecology Obstetrics & Reproductive Medicine, 2008 Prenatal diagnosis for alobar holoprosencephaly, is not difficult while for semilobar and lobar forms itmay be difficult. We present and discuss prenatal ultrasonographic and magnetic resonance imaging features of lobar holoprosencephaly in a 29 weeks ...
Evrim Erdemoğlu, Mansur Kamacı
doaj
Causes of Congenital Malformations
Pediatric Neurology Briefs, 2002 The genetic epidemiology of congenital malformations (CMs) and interaction with environmental causes are reviewed from the Arkansas Center for Birth Defects, Arkansas Children’s Hospital, Little Rock, AS.
J Gordon Millichap
doaj +1 more source