Results 201 to 210 of about 40,057 (294)

Derivative Complex Small Supernumerary Marker Chromosomes (sSMC) Involving Chromosomes 2 and 15—A Novel Report

open access: yesClinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Small supernumerary marker chromosomes (sSMC) constitute a rare group of structural chromosomal abnormalities characterized by additional genetic material that cannot be identified by conventional banding cytogenetics. The incidence of sSMC is extremely rare, and most are expected to have no clinical phenotypic abnormalities.
Yazeed Alayed   +8 more
wiley   +1 more source

A case of fetal myocardial calcification with hyperechoic area in fetal echocardiography. [PDF]

open access: yesPediatr Int
Sato T   +6 more
europepmc   +1 more source

The evolution of fetal echocardiography before and during COVID-19. [PDF]

open access: yesProg Pediatr Cardiol, 2020
Nigam P   +3 more
europepmc   +1 more source

651 Use of telemedicine in fetal echocardiography — A preliminary study

open access: bronze, 2001
Catherine Ocampo   +6 more
openalex   +1 more source

P45.06: Early fetal echocardiography with STIC technology [PDF]

open access: bronze, 2007
M. Bennásar   +6 more
openalex   +1 more source

A Rare Case of Dextrocardia With Atrioventricular Septal Defect and Situs Inversus in an 8‐Month‐Old Infant Complicated by Severe Acute Malnutrition

open access: yesClinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT The key clinical message in this case report highlights the rare coexistence of situs inversus totalis, dextrocardia, atrioventricular septal defect, and severe acute malnutrition in an Ethiopian infant. It underscores the need for heightened awareness, timely diagnosis, and integrated management strategies for such complex congenital and ...
Michael Tesfaye Kassa   +3 more
wiley   +1 more source

Extremely Rare Neonatal Case With Pyloric Atresia, Heart Defects, Hypotonia, Jaundice, and Acidosis

open access: yesClinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Pyloric atresia (PA) is an exceptionally rare congenital cause of gastric outlet obstruction, often associated with syndromic conditions such as epidermolysis bullosa (EB). This case highlights a diagnostically challenging presentation of *non‐syndromic pyloric atresia* in a neonate, complicated by a moderate mid‐muscular ventricular septal ...
Saja Abouodeh   +7 more
wiley   +1 more source

Considerations for Scaling Down Fetal Echocardiography During the COVID-19 Pandemic. [PDF]

open access: yesCan J Cardiol, 2020
Cardinal MP   +6 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy