Disease #07156 (HAE8 (angioedema, hereditary, type 8), OMIM:619367)

Official abbreviation HAE8
Name angioedema, hereditary, type 8
OMIM ID 619367
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene HS3ST6
Associated tissues -
Disease features -
Remarks -
Date created 2025-03-13 09:26:45 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00384653 - Journal: Bork 2021 Four female patients are affected, with a high number of lifetime attacks F no Germany - - - - - HAE8 Female proband fulfills the following medical criteria for diagnosing HAEnCIINH, with recurrent swellings of the skin, abdominal pain attacks, tongue swellings or laryngeal attacks; absence of urticaria; family history positive for angioedema, and normal C1-INH function and concentration in plasma HS3ST6 HS3ST6 1 4 Christian Drouet
00469720 Pat5 PubMed: Gao 2025, Journal: Gao 2025 - M no China - - - - - HAE8 HAE-nC1INH with unilateral lower extremity erysipelas, which resolved following antibiotic therapy. However, persistent, non-pitting edema developed in the same limb and subsequently progressed to the contralateral side. Symptoms persisted without improvement after administration of Icatibant and six biweekly injections of lanadelumab. HS3ST6 HS3ST6 1 1 Christian Drouet
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