Mar 3, 2025 · Polysplenia syndrome, also known as left isomerism, is a type of heterotaxy syndrome where there are multiple spleens congenitally as part of left-sided isomerism. Polysplenia is seen predominantly in female patients.

Polysplenia is a congenital disease manifested by multiple small accessory spleens, [1] rather than a single, full-sized, normal spleen. Polysplenia sometimes occurs alone, but it is often accompanied by other developmental abnormalities.

Polysplenia syndrome is a congenital disorder characterized by the presence of multiple spleens. It is associated with various risk factors, symptoms, diagnostic tests, medications, procedures, and home care strategies that can help manage the condition.

Polysplenia is a rare condition that can cause a range of symptoms in affected individuals. Some common signs of polysplenia include abdominal pain, digestive issues such as bloating or diarrhea, anemia, recurrent infections due to a weakened immune system, and …

Polysplenia syndrome (PS) is a rare condition defined as the presence of two or more spleens associated to various thoracic or abdominal abnormalities, thus defining situs ambiguous. In literature, situs ambiguous or polysplenia syndrome is …

Polysplenia syndrome refers to the association of 2 or more multiple spleens with multiple congenital abnormalities in abdomen and chest. However, some cases of polysplenia syndrome have been described with a single bilobed spleen or a single normal splenic gland.

Feb 28, 2020 · Polysplenia also called heterotaxy syndrome or bilateral left‐sidedness, is a congenital disease manifested by multiple small accessory spleens. There are frequent associated congental anomalies all related to deviations in the development of anatomical asymmetries in early embryonic stages.

Polysplenia is a multisystem congenital abnormality characterized by multiple, small splenic masses and features of bilateral left-sidedness. Accelerated curvature of the embryonic body is postulated to be a cause of polysplenia.

Polysplenia syndrome (PSS) is a rare congenital disease that associates multiple spleens to other malformations, most frequently cardiac, vascular, visceral, and biliary malformations. Most patients with PSS die in the early neonatal period because ...

Nov 16, 2016 · • Polysplenia (PSP) syndrome: Left isomerism or bilateral left-sidedness Usually multiple spleens, but may have single normal spleen – Isolated reversal of splenic position (in right abdomen) common