An unusual case of Foetal Gastroschisis with Limb aplasia and Extra-corporal liver [PDF]
, 2005 Gastroschisis represents a herniation of abdominal contents through a paramedian full-thickness abdominal fusion defect without involving the umbilical cord.
Hebbar, Shripad, N, Pratapkumar
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Unilateral submandibular gland aplasia with ipsilateral sublingual gland hypertrophy presenting as a neck mass [PDF]
, 2011 The congenital absence off the major salivary glands is a very infrequent disorder, in which several glands are usually involved at the same time. Sometimes this disorder can be associated with other developmental anomalies. The unilateral aplasia of the
Gallo Terán, J. +4 more
core +1 more source
Congenital aniridia: European COST action ANIRIDIA‐NET guidelines for diagnosis, management and care
Acta Ophthalmologica, EarlyView.Abstract Congenital aniridia is a rare ocular disorder affecting the majority of eye structures and can be associated with systemic manifestations. The main visible phenotypic characteristic is the partial or complete absence of the iris; however, foveal hypoplasia is a more frequent and reliable clinical sign. Other ocular comorbidities are associated
Davide Romano +26 more
wiley +1 more source
Variation of Posterior Communicating Artery in Human Brain – A Morphological Study
Gomal Journal of Medical Sciences, 2013 Background: The circle of Willis, present in the interpeduncular cistern at the base of the brain, is the major source of blood supply of the brain.
Anubha Saha +3 more
doaj
Rudimentary meningocele: remnant of a neural tube defect? [PDF]
, 2001 Background: Rudimentary meningocele, a malformation in which meningothelial elements are present in the skin and subcutaneous tissue, has been described in the past, under a variety of different terms and has also been referred to as cutaneous meningioma.
El Shabrawi-Caelen, Laila +5 more
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Acta Paediatrica, EarlyView.ABSTRACT Aim Urinary tract infection (UTI) is the most common and significant complication after voiding cystourethrography (VCUG) but the reported incidence in children varies highly. Therefore, the aim of this study was to evaluate the rate and possible risk factors for UTIs after VCUG. Method A multicentre retrospective cohort study of children < 15
Emelie Widhe +4 more
wiley +1 more source
Cochlear Implant Outcomes and Genetic Mutations in Children with Ear and Brain Anomalies [PDF]
, 2015 Background. Specific clinical conditions could compromise cochlear implantation outcomes and drastically reduce the chance of an acceptable development of perceptual and linguistic capabilities.
Aimoni, C +8 more
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Trasplante de médula ósea. Indicaciones y controversias.
Oncología, 2006 Presentamos el caso de una paciente de sexo femenino, 6 años de edad, con diagnóstico de leucemia aguda mieloide, en el Instituto Oncológico Dr.
Guillermo Poulson V. +3 more
doaj
Apollo Medicine, 2019 Müllerian duct aplasia–renal agenesis–cervicothoracic somite dysplasia (MURCS) association is a rare and unusual constellation of nonrandom findings that include Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia. The agenesis of
Reddy Ravikanth, Pooja Majumdar
doaj +1 more source
Identification of novel subgroup a variants with enhanced receptor binding and replicative capacity in primary isolates of anaemogenic strains of feline leukaemia virus [PDF]
, 2012 <b>BACKGROUND:</b> The development of anaemia in feline leukaemia virus (FeLV)-infected cats is associated with the emergence of a novel viral subgroup, FeLV-C.
A Manrique +58 more
core +3 more sources