Infantile Hyperchylomicronemia Due to A Novel GPIHBP1 Disease-Causing Variant Presenting with Milky Blood: A Rare Case Report
Background: Familial hyperchylomicronemia is a very rare autosomal recessive disorder and the most severe type of pediatric hyperlipidemia. The purpose of this case report is to enhance clinician's insight on the diagnosis and management plan in the case of infantile hyperchylomicronemia presenting...
সংরক্ষণ করুন:
| প্রধান লেখক: | , , , , , |
|---|---|
| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
Indonesian Society of Pediatric Gastroenterology, Hepatology, and Nutrition
2023-05-01
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| মালা: | Archives of Pediatric Gastroenterology, Hepatology, and Nutrition |
| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://apghn.com/index.php/journal/article/view/33 |
| ট্যাগগুলো: |
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