Results 81 to 90 of about 20,124 (268)
Duodenal obstruction due to a preduodenal portal vein
African Journal of Paediatric Surgery, 2014 An infant presented with clinical signs and symptoms suggestive of a pyloric stenosis. On abdominal ultrasound, pyloric stenosis was excluded, and other causes for proximal duodenal obstruction, such as a duodenal web or annular pancreas, were suspected.
MNC Vilakazi +4 more
doaj +1 more source
A new conceptual framework for investigating complex genetic disease [PDF]
, 2015 Some common diseases are known to have an inherited component, however their population- and familial-incidence patterns do not conform to any known monogenic Mendelian pattern of inheritance and instead they are currently much better explained if an ...
Shobbir Hussain
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American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff +8 more
wiley +1 more source
Hypertrophic pyloric stenosis treated with co-administration of nitroglycerin and atropine sulfate
Journal of Pediatric Surgery Case Reports, 2018 Hypertrophic pyloric stenosis (HPS) is a common infantile disease that causes a transit pyloric disorder. For the treatment of this disorder, intravenous atropine sulfate (AS) has been reported to be effective.
Yoko Shino +4 more
doaj +1 more source
Sténose hypertrophique du pylore Etude comparative rétrospective post-pyloromyotomie extramuqueuse des modes de réalimentation post- opératoires [PDF]
, 2015 La sténose hypertrophique du pylore (SHP) est une maladie fréquente chez les nourrissons âgés de quelques semaines. Son étiologie reste inconnue. Elle se manifeste par des vomissements en jet et une perte pondérale.
ZBINDEN, O.
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Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature
American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim +2 more
wiley +1 more source
, 2010 We have reported a case of Yunis-Varon syndrome which is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones, characteristic facial features, abnormalities of the fingers and/or toes ...
Dal, SI, Parmar, P
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Eosinofiilne gastroenteriit seedetrakti vaevuste ühe põhjusena [PDF]
, 2004 Eosinofiilne gastroenteriit on harva esinev, täpselt teadmata põhjuse ja tekkemehhanismiga, ägenemiste ning remissioonidega kulgev krooniline haigus. Sellele haigusele on iseloomulik seedetrakti erinevate vaevuste ja sümptomite esinemine,
Ress, Krista, Uibo, Oivi
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CNS Neuroscience &Therapeutics, Volume 31, Issue 12, December 2025.As requested, we provide the graphical abstract text below. Once approved, we will insert it into the manuscript (Word file):“This review outlines the immune–inflammatory interactions linking atherosclerosis and ischemic stroke, highlights emerging mechanistic pathways, and summarizes potential translational targets across both vascular diseases ...
Hongdong Hao +7 more
wiley +1 more source
Wolff-Parkinson-White syndrome in an adolescent with depression [PDF]
, 2016 Wolff-Parkinson-White (WPW) syndrome is a congenital disorder characterised by a macro-reentrant arrhythmia caused by preexcitation of the ventricles.
Chen, Fei +4 more
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