Results 101 to 110 of about 10,496 (209)

An Evolutionarily Conserved Network Mediates Development of the zona limitans intrathalamica, a Sonic Hedgehog-Secreting Caudal Forebrain Signaling Center

Journal of Developmental Biology, 2016
Recent studies revealed new insights into the development of a unique caudal forebrain-signaling center: the zona limitans intrathalamica (zli). The zli is the last brain signaling center to form and the first forebrain compartment to be established.
Elena Sena, Kerstin Feistel, Béatrice C. Durand   +2 more
doaj   +1 more source

The acrocallosal syndrome: A case report and literature survey [PDF]

, 2009
Acrocallosal syndrome (ACS) is a rare, genetically transmitted disorder characterized by facial deformities. These include a large forehead, large anterior fontanelle, broad nasal bridge with increased intercanthal distance, partial or complete agenesis ...
Davies, Lindsey, Gonzales, Cesar, Hodgson, Brian   +2 more
core   +1 more source

Aplicación clínica de las imágenes de resonancia potenciadas en difusión y tractografía en un niño con holoprosencefalia

Biomédica: revista del Instituto Nacional de Salud, 2011
Las imágenes de resonancia magnética potenciadas en difusión y tractografía pueden emplearse en el estudio de las malformaciones congénitas del sistema nervioso central asociadas a anormalidades en los tractos de sustancia blanca. Presentamos un paciente
Blair Ortiz, Diego A. Herrera, Sergio Vargas   +2 more
doaj   +1 more source

Arthrogryposis: A Rare Manifestation in Infant of Diabetic Mother [PDF]

, 2009
Arthrogryposis multiplex congenita is characterized by non-progressive, multiple joint contractures present at birth. The major cause of arthrogryposis is fetal akinesia due to fetal abnormalities like neurogenic, muscle, connective tissue abnormalities ...
Kumar, Arvind, Taksande, AM, Vilhekar, KY   +2 more
core  

A male fetus with cyclopia was discovered after miscarriage: A rare case report from Syria

Clinical Case Reports
Key Clinical Message This case of alobar holoprosencephaly and cyclopia emphasizes the value of prenatal check‐ups, particularly in low‐income countries.
Tala Dakkak, Marah Mansour, Habib Jarbouh, Abdolmoin Ktail   +3 more
doaj   +1 more source

Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritance

The Turkish Journal of Pediatrics, 2008
Pseudo-trisomy 13 is defined in chromosomally normal patients with holoprosencephaly and associating features suggestive of trisomy 13. An autosomal recessive pattern of inheritance for this situation is most likely, but a gene for this condition ...
G Eda Utine, Yasemin Alanay, Dilek Aktaş, Beril Talim, Gülsev Kale, Ergül Tunçbilek   +5 more
doaj  

Holoprosencephaly

Neurologia medico-chirurgica, 1978
K, Osaka, T, Tanimura, S, Yamasaki, A, Hirayama, K, Fujita, S, Matsumoto   +5 more
openaire   +3 more sources

Fetal midline anomalies: Diagnosis and counselling part 2: Septal anomalies. [PDF]

, 2018
D'Antonio, F, Khalil, A, Leombroni, M, Liberati, M   +3 more
core   +1 more source

Detailed Analysis of Fetal Malformations of the Supratentorial Structures of the Brain in High-Risk Pregnancies at 12–14 Gestational Weeks by Transvaginal 3D Ultrasound Examination

Ultrasound International Open
Purpose  To detect sonographic abnormalities of the supratentorial structures of the brain – future cavum septum pellucidum, cavum velum interpositum, third ventricle, ganglionic eminence and thalamus ...
Reinhard Altmann, Iris Scharnreitner, Sabine Enengl, Patrick Stelzl, Peter Oppelt, Elisabeth Reiter   +5 more
doaj   +1 more source

A preterm infant with semilobar holoprosencephaly and hydrocephalus: a case report [PDF]

, 2010
Ashish O Gupta, Patrick Leblanc, Krishna C Janumpally, Pattaraporn Tanya   +3 more
core   +1 more source