# “No End Point Detected”: A Unique Coagulation Profile Unmasking Dysfibrinogenemia

## TL;DR

A rare fibrinogen disorder was diagnosed in a young woman with abnormal coagulation tests and severe bleeding during pregnancy.

## Contribution

A unique coagulation profile with 'no end point detected' is highlighted as a diagnostic clue for dysfibrinogenemia.

## Key findings

- Abnormal PT, PTT, and Clauss fibrinogen assays indicated a fibrinogen disorder.
- Fibrinogen replacement normalized coagulation tests and confirmed the diagnosis.
- A pathogenic FGB variant supported the diagnosis of dysfibrinogenemia.

## Abstract

Dysfibrinogenemia is a rare qualitative fibrinogen disorder that can present with bleeding, thrombosis, or both. We report a case of a young woman with first-trimester pregnancy loss and severe hemorrhage, whose coagulation tests reported “no end point detected” on PT, PTT, and Clauss fibrinogen assays. This pattern should prompt consideration of profound hypofibrinogenemia or qualitative fibrinogen defects. Fibrinogen replacement normalized PT and PTT and yielded measurable fibrinogen levels, enabling definitive diagnosis. Discordant activity and antigen levels, along with a pathogenic FGB variant, confirmed dysfibrinogenemia. This case underscores the importance of considering fibrinogen disorders in uninterpretable coagulation profiles and initiating early replacement.