Results 181 to 190 of about 11,012 (235)
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Prenatal Diagnosis, 2022
Parents receiving a prenatal diagnosis of alobar holoprosencephaly (HPE) often experience uncertainty regarding the pregnancy prognosis. There is little known about how best to counsel and support families receiving the diagnosis.
Hunaydah Elfarawi +4 more
semanticscholar +1 more source
Parents receiving a prenatal diagnosis of alobar holoprosencephaly (HPE) often experience uncertainty regarding the pregnancy prognosis. There is little known about how best to counsel and support families receiving the diagnosis.
Hunaydah Elfarawi +4 more
semanticscholar +1 more source
Prenatal diagnosis of holoprosencephaly
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 2018Youssef A Kousa
exaly +2 more sources
Sonography of fetal holoprosencephaly: a guide to recognize the lesser varieties
Journal of Maternal-Fetal & Neonatal Medicine, 2022Background Alobar holoprosencephaly (HPE) is easily detected during a first-trimester screening examination, conversely, recognizing the lesser varieties may be difficult even in the second trimester.
E. Montaguti +6 more
semanticscholar +1 more source
International Journal of Paleopathology, 2021
OBJECTIVE This study presents evidence of a probable case of holoprosencephaly with cyclopia, which has been rarely reported in the paleopathological literature.
A. Palamenghi +4 more
semanticscholar +1 more source
OBJECTIVE This study presents evidence of a probable case of holoprosencephaly with cyclopia, which has been rarely reported in the paleopathological literature.
A. Palamenghi +4 more
semanticscholar +1 more source
Holoprosencephaly flashcards: A summary for the clinician
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 2010 International audienceThis material contains general information regarding the approach to patients with holoprosencephaly.
Maximilian Muenke
exaly +2 more sources
Journal of Child Neurology, 2020
Holoprosencephaly is the most common malformation of forebrain development and includes a wide spectrum of severity. The objective of this retrospective study was to evaluate fetal magnetic resonance imaging (MRI) associations with outcome.
Artur Riddle +4 more
semanticscholar +1 more source
Holoprosencephaly is the most common malformation of forebrain development and includes a wide spectrum of severity. The objective of this retrospective study was to evaluate fetal magnetic resonance imaging (MRI) associations with outcome.
Artur Riddle +4 more
semanticscholar +1 more source
International Journal of Pediatric Otorhinolaryngology, 1994
A single nostril associated with alobar holoprosencephaly is a rare congenital lesion. This paper reports two female term neonates with holoprosencephaly. The first neonate asphyxiated at birth had a single nostril, hypotelorism, posterior cleft palate, inferonasal coloboma of the iris and disc and persistent tunica vasculosa lentis.
S P, Ram +3 more
openaire +2 more sources
A single nostril associated with alobar holoprosencephaly is a rare congenital lesion. This paper reports two female term neonates with holoprosencephaly. The first neonate asphyxiated at birth had a single nostril, hypotelorism, posterior cleft palate, inferonasal coloboma of the iris and disc and persistent tunica vasculosa lentis.
S P, Ram +3 more
openaire +2 more sources
Holoprosencephaly with Proboscis
Gynecologic and Obstetric Investigation, 2010This is the case of a male newborn with holoprosencephaly, marked hypotelorism, and a rudimentary nasal structure, the proboscis. The head CT scan showed a single monoventricle and two ocular globes fused at the midline. Chromosome studies showed a normal karyotype.
M, Galguera, L, Malave, A, Leon
openaire +2 more sources
The Indian Journal of Pediatrics, 2004
To conduct a clinical study of holoprosencephaly (HPE).Thirteen cases of HPE were studied regarding their clinical features, family history, and prenatal and imaging studies. Chromosomal analysis was done whenever fresh sample was available.Six cases were antenatally detected by ultrasound; four cases were stillborn.
Seema, Thakur +3 more
openaire +2 more sources
To conduct a clinical study of holoprosencephaly (HPE).Thirteen cases of HPE were studied regarding their clinical features, family history, and prenatal and imaging studies. Chromosomal analysis was done whenever fresh sample was available.Six cases were antenatally detected by ultrasound; four cases were stillborn.
Seema, Thakur +3 more
openaire +2 more sources
Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations
Prenatal Diagnosis, 2020The objective of this study is to evaluate the prenatal diagnosis, postnatal characteristics, and the spectrum of associated findings in fetuses with holoprosencephaly (HPE).
Sara H. El-Dessouky +11 more
semanticscholar +1 more source