Results 121 to 130 of about 167,788,531 (210)

Corpus callosum agenesis [PDF]

, 2020
openaire   +2 more sources

Clinical Presentation of Agenesis of Corpus Callosum Among Children in a Single Tertiary Care Center in Riyadh, Saudi Arabia. [PDF]

Cureus
Altwaijri W, Bajaman RS, Almutairi MG, Alomary AA, Alzuhair SK, Alhudaif LO.   +5 more
europepmc   +1 more source

Anomalies on anterior and posterior complex views in fetuses with partial agenesis of corpus callosum. [PDF]

Ultrasound Obstet Gynecol
Viñals F, Correa F, García-Rodríguez R, Tubau-Navarra A, Esparza M, Diaz L.   +5 more
europepmc   +1 more source

Lissencephaly with agenesis of corpus callosum: A rare anomaly. [PDF]

Med J Armed Forces India, 2016
Maurya VK, Bhatia M, Ravikumar R, Senger KP.   +3 more
europepmc   +1 more source

Fetal agenesis of corpus callosum: chromosomal copy number abnormalities and postnatal follow-up. [PDF]

Mol Biol Rep
Cai M, Lin N, Fu M, Que Y, Huang H, Xu L.   +5 more
europepmc   +1 more source

Patent Ductus Arteriosus in Association With Agenesis of Corpus Callosum: Syndromic Links, Difficult Airway Challenges, and Pediatric Anesthesia Management. [PDF]

Cureus
Sawant U, Sen J, Wadaskar D.
europepmc   +1 more source

Dandy Walker variant with agenesis of corpus callosum diagnosed late prenatally by foetal ultrasound: a case report. [PDF]

Ann Med Surg (Lond)
Paudel S, Poudel SK, Shah R, Regmi S, Zoowa R.   +4 more
europepmc   +1 more source

Do we consider Andermann syndrome in infants with agenesis of corpus callosum

, 2003
Do we consider Andermann syndrome in infants with agenesis of corpus callosum: Andermann syndrome is characterized by agenesis of corpus callosum, anterior horn cell disease, a mixed sensory and motor neuropathy, and facial dysmorphism, and is inherited ...
Caksen, H, Icagasioglu, D, Deda, G
core  

Rare Triad of Midline Craniofacial Defects: A Case Report

Journal of Craniomaxillofacial Research
Midline craniofacial anomalies are rare malformations that may occur in isolation or as part of syndromic associations. Among them, the coexistence of basal encephalocele, agenesis of the corpus callosum, and Morning Glory Syndrome (MGS) is exceptionally
Praveen Thirumal, Ramakrishna N, Sai Praneetha Sagi   +2 more
doaj  

Identification of a Novel CDH2 Gene Variant in an ACOGS Patient with Concurrent Respiratory Tract Infection: A Case Report. [PDF]

Pediatric Health Med Ther
Lu Y, Fang F, Zhou H, Shu S, Liu X.
europepmc   +1 more source