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Upshaw-Schulman Syndrome with a Novel Deletion in Exon 17 of ADAMTS 13 Gene. | LitMetric

Upshaw-Schulman Syndrome with a Novel Deletion in Exon 17 of ADAMTS 13 Gene.

Indian J Pediatr

Department of Pediatrics, Armed Forces Medical College, Pune, Maharashtra, 411040, India.

Published: April 2022

AI Article Synopsis

  • Upshaw-Schulman syndrome is a rare congenital disorder linked to thrombotic thrombocytopenic purpura (TTP), marked by episodes of low platelet counts, hemolytic anemia, and microvascular clots causing organ damage, especially in the kidneys, heart, and brain.
  • A 6-month-old infant from a consanguineous family experienced severe jaundice and thrombocytopenia, prompting urgent medical intervention, including exchange transfusion and later, fresh frozen plasma (FFP) transfusions.
  • Genetic testing confirmed the diagnosis of congenital TTP by identifying a specific mutation in the ADAMTS 13 gene, indicating an autosomal recessive inheritance pattern.

Article Abstract

Upshaw-Schulman syndrome is a rare congenital form of thrombotic thrombocytopenic purpura (TTP) characterized by single or recurrent episodes of thrombocytopenia, microangiopathic hemolyticanemia (MAHA), and widespread microvascular thrombosis, leading to the ischemic damage of multiple organs (mainly kidney, heart and brain). A 6-mo-old female infant, second born of a third-degree consanguineous marriage, with a history of severe neonatal jaundice with thrombocytopenia secondary to hemolysis requiring exchange transfusion on day 2 of life, presented with high-grade fever without focus of 2-d duration. Initial workup revealed microangiopathic hemolyticanemia with thrombocytopenia. In view of microangiopathic hemolyticanemia with thrombocytopenia against a background of severe neonatal jaundice, a diagnosis of congenital TTP was considered and was managed with FFP transfusion. The diagnosis was confirmed with her exome sequencing showing autosomal recessive homozygous frameshift deletion c.2063delG (p.Trp688fs) at Exon 17 (NM_139025) of ADAMTS 13 gene.

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Source
http://dx.doi.org/10.1007/s12098-021-04047-2DOI Listing

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