Results 61 to 70 of about 1,285 (112)
The Turkish Journal of Pediatrics, 2000 An 8 1/2-month-old girl with biliary atresia and polysplenia syndrome having multiple vascular anomalies without cardiac anomalies is reported. Interruption of the inferior vena cava with azygous continuation, which is a common anomaly, was seen ...
N C Tarhan +4 more
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A very rare case of polysplenia syndrome with congenital diffuse pulmonary arteriovenous fistulas
The Turkish Journal of Pediatrics, 2006 A five-year-old girl patient was admitted with cyanosis and dyspnea, which started from birth. She had small telangiectatic lesions on her face and cerebral arteriovenous malformation, but no family history of hereditary hemorrhagic telangiectasia.
Dolunay Gürses +3 more
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The Successful Management of Gangrenous Pneumococcal Infection in an Infant With Polysplenia Syndrome. [PDF]
Cureus, 2023 Garout W.
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Polysplenia Syndrome Complicated by Splenic Infarction: A Report of a Rare Case. [PDF]
Cureus, 2023 Abdullah RA +5 more
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Archives of Endocrinology and MetabolismSUMMARY Heterotaxy syndrome (HS) is a rare congenital condition with multifactorial heritance, characterized by an abnormal arrangement of thoraco-abdominal organs and vessels.
Cínthia Minatel Riguetto +2 more
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Polysplenia syndrome revealed in adulthood by pancreatic and vascular malformations: a case report. [PDF]
Pan Afr Med J, 2022 Mountassir ME +5 more
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Polysplenia syndrome in adulthood: a case report. [PDF]
Pan Afr Med J, 2022 Malki MC +9 more
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Syndromic variants of biliary atresia
World Journal of Pediatric SurgeryBiliary atresia (BA) may be characterized as an obliterative cholangiopathy presenting in the newborn period with conjugated jaundice, pale stools, and dark urine. It is usually thought of as an isolated anomaly in otherwise normal infants. However, in a
Mark Davenport
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