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Congenital hypofibrinogenemia with bone cyst: a case report with review of literature

Year: 2024

Type: article

Abstract: Congenital hypofibrinogenemia is a rare autosomal recessive condition leading to low plasma fibrinogen levels, affecting approximately one in a million. The clinical phenotype is diverse and may vary from bleeding and thrombosis to the absence of symptoms. Bone cysts are an infrequent complication of hypofibrinogenemia. This case report describes the clinical history, diagnosis, and treatment of a 13-year-old patient with congenital hypofibrinogenemia with a bone cyst.

Source: Revista Hematología

DOI: 10.48057/hematologa.v28i2.579

Authors: M Mamadapur, V Yelugoti

Institutions: JSS Medical College and Hospital, Madras Medical College

Language: English

Topic: Blood properties and coagulation

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: diamond

OpenAlex ID: W4402030437

FWCI:

Cites: 10

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Related to: 10