Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kanya Singhapakdi"'
Publikováno v:
Case Reports in Cardiology, Vol 2023 (2023)
Several congenital anomalies of the right atrial appendage (RAA) have been described including aneurysm, herniation (in association with a pericardial defect), and left juxtaposition. The left juxtaposition of the RAA (LJRAA), first described by Birm
Externí odkaz:
https://doaj.org/article/0cbaa981cb894802a7a7084bbfc27c1a
Publikováno v:
Journal of Pediatric Neurology. 19:377-383
X-linked adrenoleukodystrophy (ALD) is a leukodystrophy characterized not only by progressive loss of myelin in the central nervous system due to dysmyelination, but also by acute, subacute, or chronic inflammatory demyelination. This results in the
Autor:
Kanya Singhapakdi, Paul Maertens
Publikováno v:
Journal of Pediatric Neurology. 19:264-269
Gratification disorder (GD) is a form of stereotyped posturing with mechanical pressure applied to the genitalia without manual manipulation and is generally considered benign. Here, we describe two patients who exhibited GD. Both were later diagnose
Publikováno v:
Journal of neuroimaging : official journal of the American Society of NeuroimagingREFERENCES. 32(3)
Congenital lymphocytic choriomeningitis virus (LCMV) infection is a transient intrauterine viral infection with selective teratogenicity depending on the timing of the primary maternal infection. LCMV is cleared from the body of the fetus after the a
Autor:
Peter B. Soh, Kanya Singhapakdi, Juan C. Gonzalez, Ramachandra Bhat, Paul Maertens, Om Prakash Jha
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 37(1)
Congenital anophthalmia is rare and can occur due to various etiologies, including genetic defects, teratogenic exposures, and vascular disruptions. We report a rare case of right-sided congenital anophthalmia and hemicerebral dysgenesis in associati
Publikováno v:
Journal of Pediatric Neurosciences
Schizencephaly is a rare type of neuronal migration disorder characterized by the presence of a cerebral hemispheric cleft that extends from lateral ventricles to the cortical surface of the brain. We report a rare case of prenatally diagnosed unilat