Results 81 to 90 of about 30,638 (241)
Central precocious puberty in a 3 year-old girl with Phenylketonuria: a rare association? [PDF]
, 2014 Background Central precocious puberty (CPP) and phenylketonuria (PKU) are two rare conditions, the latter being the rarer. To date, only one case featuring both these conditions has been reported, and hyperphenylalaninemia was assumed triggering CPP.
Donaldson, Malcolm +3 more
core +3 more sources
Multiple Choriangiomas of Placenta [PDF]
, 2011 Placental chorangiomas, not an uncommon condition is often small and hence usually goes unnoticed . However the incidence of complications is high when the chorangioma is large. We hereby present an unusual case of large and multiple choriangiomas with
Krishnan, Nalini +4 more
core +1 more source
Veterinary Dermatology, EarlyView.ABSTRACT A 5‐year‐old female cat presented with a purple depressed lesion on a metatarsal pad inducing ulceration and pain. Histopathological results revealed a non‐neoplastic vascular proliferation, a rare condition in cats. Topical beta‐blocker successfully prevented recurrence of ulceration.
Adrien Accard +6 more
wiley +1 more source
Adenomyoma of the small intestine a rare pathological lead point for intussusception in an infant [PDF]
, 2014 INTRODUCTION: Intussusception is a typical abdominal emergency in early childhood. CASE DESCRIPTION: We report a case of an infant in the typically affected age group with an intussusception triggered by a rare benign intramural intestinal adenomyoma as ...
Henning C Fiegel +3 more
core +1 more source
هامارتوم کندروييد قفسه سينه در نوزادی: گزارش يک مورد نادر [PDF]
, 2010 مقدمه: هامارتوم کندروييد قفسه سينه، تومور خوش خيم بسيار نادری است که معمولاً هنگام تولد يا در ابتدای دوران کودکی بروز مييابد. اين بيماری غالباً بهصورت يک توده قابل لمس در جدار قفسه سينه تظاهر مييابد.
جهانگيری, فریبا +3 more
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Multimodale Bildgebung eines retinalen Astrozyten-Hamartoms assoziert mit angeborener Hypertrophie des retinalen Pigmentepithels [Multimodal Imaging of Retinal Astrocytic Hamartoma Associated with Congenital Hypertrophy of Retinal Pigment Epithelium] [PDF]
, 2016 Hamartoma is a nodular malformation, with a single or multiple malformations, it is a recognized prenatal developmental abnormality. This benign tumor lesion has the same histological components of normal parenchyma, but these components are arranged ...
De Ancos, E. +5 more
core +1 more source
Pregnancy, Volume 2, Issue 3, May 2026.Abstract Background Polyhydramnios, megalencephaly, and symptomatic epilepsy (PMSE) syndrome is a rare autosomal recessive mTORopathy caused by biallelic STE20‐related kinase adaptor alpha (STRADA) loss‐of‐function variants. Animal models demonstrate that in utero mechanistic target of rapamycin (mTOR) inhibition can prevent cortical dyslamination ...
Christian Macedonia +5 more
wiley +1 more source
Hamartoma mesenquiamal hepático m crianças: relato de dois casos. [PDF]
, 2003 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Prestes, Fábio Xavier
core
Veterinary Record Case Reports, Volume 14, Issue 2, May 2026.Abstract An 11‐week‐old Holstein Friesian heifer calf presented with a congenital nasal abnormality characterised by an additional, turbinate‐like structure located dorsally on the nasal bridge. Clinical examination of the calf revealed normal respiratory function, with the accessory structure producing mucoid discharge from blind‐ended cavities ...
Raffaela Marian +4 more
wiley +1 more source