Results 181 to 190 of about 12,857 (288)
A rare cause of deep vein thrombosis: inferior vena cava agenesis. [PDF]
Del Canto Peruyera P +1 more
europepmc +1 more source
ABSTRACT Anterior sacral meningocele (ASM) is an uncommon congenital spinal abnormality in which the meningeal sac herniates through an abnormality in the anterior sacrum into the presacral space. It is more observed in females and usually asymptomatic; large ASMs may cause pressure effects on nearby pelvic structures. A 30‐year‐old male presented with
Ayesha Farooq +7 more
wiley +1 more source
ABSTRACT Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutations. It classically manifests with renal hypodysplasia and optic nerve anomalies. However, recent literature suggests an expanding phenotypic spectrum.
Nadira Sultana +2 more
wiley +1 more source
ABSTRACT Objectives Uterine Sensitization‐Associated Gene 1 (USAG‐1) is a bone morphogenetic protein (BMP) antagonist vital for tooth regeneration that is expressed in kidney, gingiva, and dental tissues. Material and methods We analyzed recent studies focusing on USAG‐1 and its involvement in BMP and Wnt signaling pathways related to dental tissue ...
Zahra Moradi +9 more
wiley +1 more source
Agenesis of the Left Pulmonary Artery, as Incidental Finding. [PDF]
Jiménez Romero AA +5 more
europepmc +1 more source
ABSTRACT To determine whether TXNDC15 variation causes Meckel–Gruber syndrome (MKS), we assessed the pathogenicity of the frameshift variant c.560delA. A CRISPR–Cas9 generated mouse model carrying the equivalent Txndc15 c.512delA mutation was analyzed at embryonic day 15.5.
Yang Liu +10 more
wiley +1 more source
ABSTRACT Objective To describe prenatal imaging findings and postnatal outcomes in fetuses diagnosed with saccular forms of closed spinal dysraphism (CSD). Methods This retrospective single‐centre study included fetuses diagnosed with non‐genetic, non‐syndromic CSD between January 2018 and June 2023.
Yada Kunpalin +8 more
wiley +1 more source
Nutritional approach in a growing Jack Russell terrier with gall bladder agenesis
Abstract An asymptomatic male Jack Russell terrier diagnosed at the age of 18 weeks with congenital gall bladder agenesis, confirmed by computed tomography scan, after finding abnormally high values for liver enzymes in a routine blood count. Treatment with liver‐protective agents S‐adenosylmethionine and ursodeoxycholic acid was initiated. At 6 months
Tamara Seghers +3 more
wiley +1 more source
[ Giant asymptomatic anterolateral diaphragmatic hernia in an adult: report of a rare case] [PDF]
Espana MI +3 more
europepmc +1 more source
Agenesia parcial del cuerpo calloso en una infante
Se presenta el caso clínico de una infante de 13 meses de edad, con antecedente de agenesia del cuerpo calloso, quien ingresó en la sala de nutrición del Hospital General Docente "Dr.
Julio Ernesto Rodríguez Serret +2 more
doaj

