{"product_id":"congenital-afibrinogenemia-gene-panel","title":"Congenital afibrinogenemia gene panel","description":"\u003cp\u003eAmniotic Fluid\/ Chorionic Villus Sample\/Peripheral Venous Blood\/Cord blood,\/Extracted DNA\/Dry Blood Spot\u003c\/p\u003e\n\u003cdiv class=\"qMYqUG_convSearchResultHighlightRoot\"\u003e\n\u003cdiv class=\"\" data-turn-id-container=\"eafb3547-f64a-4b6b-a45d-233d222644f7\" data-is-intersecting=\"true\"\u003e\n\u003csection class=\"text-token-text-primary w-full focus:outline-none has-data-writing-block:pointer-events-none [\u0026amp;:has([data-writing-block])\u0026gt;*]:pointer-events-auto R6Vx5W_threadScrollVars scroll-mb-[calc(var(--scroll-root-safe-area-inset-bottom,0px)+var(--thread-response-height))] scroll-mt-(--header-height)\" dir=\"auto\" data-turn-id=\"eafb3547-f64a-4b6b-a45d-233d222644f7\" data-turn-id-container=\"eafb3547-f64a-4b6b-a45d-233d222644f7\" data-testid=\"conversation-turn-1\" data-scroll-anchor=\"false\" data-turn=\"user\"\u003e\u003c\/section\u003e\n\u003cbr\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"\" data-turn-id-container=\"request-WEB:c1fd3cc1-079e-49d4-a82f-6e2700a5ddac-3\" data-is-intersecting=\"true\"\u003e\n\u003csection class=\"text-token-text-primary w-full focus:outline-none has-data-writing-block:pointer-events-none [\u0026amp;:has([data-writing-block])\u0026gt;*]:pointer-events-auto R6Vx5W_threadScrollVars scroll-mb-[calc(var(--scroll-root-safe-area-inset-bottom,0px)+var(--thread-response-height))] scroll-mt-[calc(var(--header-height)+min(200px,max(70px,20svh)))]\" dir=\"auto\" data-turn-id=\"request-WEB:c1fd3cc1-079e-49d4-a82f-6e2700a5ddac-3\" data-turn-id-container=\"request-WEB:c1fd3cc1-079e-49d4-a82f-6e2700a5ddac-3\" data-testid=\"conversation-turn-2\" data-scroll-anchor=\"false\" data-turn=\"assistant\"\u003e\n\u003cdiv class=\"text-base my-auto mx-auto pb-10 [--thread-content-margin:var(--thread-content-margin-xs,calc(var(--spacing)*4))] @w-sm\/main:[--thread-content-margin:var(--thread-content-margin-sm,calc(var(--spacing)*6))] @w-lg\/main:[--thread-content-margin:var(--thread-content-margin-lg,calc(var(--spacing)*16))] px-(--thread-content-margin)\"\u003e\n\u003cdiv class=\"[--thread-content-max-width:40rem] @w-lg\/main:[--thread-content-max-width:48rem] mx-auto max-w-(--thread-content-max-width) flex-1 group\/turn-messages focus-visible:outline-hidden relative flex w-full min-w-0 flex-col agent-turn\"\u003e\n\u003cdiv class=\"flex max-w-full flex-col gap-4 grow\"\u003e\n\u003cdiv data-message-author-role=\"assistant\" data-message-id=\"0b076532-93a8-4aa2-9b3c-2e04a2fb8025\" dir=\"auto\" data-message-model-slug=\"gpt-5-5\" class=\"min-h-8 text-message relative flex w-full flex-col items-end gap-2 text-start break-words whitespace-normal outline-none keyboard-focused:focus-ring [.text-message+\u0026amp;]:mt-1\" data-turn-start-message=\"true\" tabindex=\"0\"\u003e\n\u003cdiv class=\"flex w-full flex-col gap-1 empty:hidden\"\u003e\n\u003cdiv class=\"markdown prose dark:prose-invert wrap-break-word w-full light markdown-new-styling\"\u003e\n\u003ch2 data-section-id=\"1jtviim\" data-start=\"0\" data-end=\"40\"\u003eCongenital Afibrinogenemia Gene Panel\u003c\/h2\u003e\n\u003ch3 data-section-id=\"2f5clp\" data-start=\"42\" data-end=\"81\"\u003eWhat is Congenital Afibrinogenemia?\u003c\/h3\u003e\n\u003cp data-start=\"82\" data-end=\"424\"\u003eCongenital Afibrinogenemia is a rare inherited bleeding disorder where the body is unable to produce enough fibrinogen — an essential protein needed for blood clot formation. Individuals with this condition may experience excessive bleeding, delayed wound healing, easy bruising, nosebleeds, gum bleeding, or bleeding after surgery or trauma.\u003c\/p\u003e\n\u003ch3 data-section-id=\"1qm60ho\" data-start=\"426\" data-end=\"458\"\u003eWhy is this Gene Panel Done?\u003c\/h3\u003e\n\u003cp data-start=\"459\" data-end=\"567\"\u003eThis genetic test helps identify mutations associated with inherited fibrinogen disorders. It is useful for:\u003c\/p\u003e\n\u003cul data-start=\"569\" data-end=\"822\"\u003e\n\u003cli data-section-id=\"70i2al\" data-start=\"569\" data-end=\"630\"\u003eDiagnosing congenital afibrinogenemia or hypofibrinogenemia\u003c\/li\u003e\n\u003cli data-section-id=\"em7qwc\" data-start=\"631\" data-end=\"674\"\u003eIdentifying hereditary bleeding disorders\u003c\/li\u003e\n\u003cli data-section-id=\"o0bgzu\" data-start=\"675\" data-end=\"715\"\u003eFamily screening and carrier detection\u003c\/li\u003e\n\u003cli data-section-id=\"ggs57h\" data-start=\"716\" data-end=\"765\"\u003eGenetic counseling and prenatal risk assessment\u003c\/li\u003e\n\u003cli data-section-id=\"1df5m3z\" data-start=\"766\" data-end=\"822\"\u003eSupporting treatment planning and long-term management\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"lkqztw\" data-start=\"824\" data-end=\"851\"\u003eGenes Commonly Analyzed\u003c\/h3\u003e\n\u003cp data-start=\"852\" data-end=\"895\"\u003eThe panel primarily evaluates mutations in:\u003c\/p\u003e\n\u003cul data-start=\"897\" data-end=\"926\"\u003e\n\u003cli data-section-id=\"d6cdag\" data-start=\"897\" data-end=\"906\"\u003e\u003cstrong data-start=\"899\" data-end=\"906\"\u003eFGA\u003c\/strong\u003e\u003c\/li\u003e\n\u003cli data-section-id=\"d6ce2z\" data-start=\"907\" data-end=\"916\"\u003e\u003cstrong data-start=\"909\" data-end=\"916\"\u003eFGB\u003c\/strong\u003e\u003c\/li\u003e\n\u003cli data-section-id=\"d6ci8e\" data-start=\"917\" data-end=\"926\"\u003e\u003cstrong data-start=\"919\" data-end=\"926\"\u003eFGG\u003c\/strong\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp data-start=\"928\" data-end=\"995\"\u003eThese genes are responsible for fibrinogen production and function.\u003c\/p\u003e\n\u003ch3 data-section-id=\"ik3d6w\" data-start=\"997\" data-end=\"1016\"\u003eRecommended For\u003c\/h3\u003e\n\u003cp data-start=\"1017\" data-end=\"1063\"\u003eThis test may be advised for individuals with:\u003c\/p\u003e\n\u003cul data-start=\"1065\" data-end=\"1261\"\u003e\n\u003cli data-section-id=\"jylcwj\" data-start=\"1065\" data-end=\"1106\"\u003eUnexplained recurrent bleeding episodes\u003c\/li\u003e\n\u003cli data-section-id=\"1rz8mbf\" data-start=\"1107\" data-end=\"1132\"\u003eProlonged clotting time\u003c\/li\u003e\n\u003cli data-section-id=\"g611vg\" data-start=\"1133\" data-end=\"1171\"\u003eFamily history of bleeding disorders\u003c\/li\u003e\n\u003cli data-section-id=\"zmx0p\" data-start=\"1172\" data-end=\"1205\"\u003eNeonatal bleeding complications\u003c\/li\u003e\n\u003cli data-section-id=\"76ujyn\" data-start=\"1206\" data-end=\"1261\"\u003eExcessive bleeding after surgery or dental procedures\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"11twy89\" data-start=\"1263\" data-end=\"1282\"\u003eSample Required\u003c\/h3\u003e\n\u003cul data-start=\"1283\" data-end=\"1308\"\u003e\n\u003cli data-section-id=\"1ch15qg\" data-start=\"1283\" data-end=\"1308\"\u003ePeripheral Blood Sample\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"kvtkvb\" data-start=\"1310\" data-end=\"1329\"\u003eTechnology Used\u003c\/h3\u003e\n\u003cul data-start=\"1330\" data-end=\"1364\"\u003e\n\u003cli data-section-id=\"oumte0\" data-start=\"1330\" data-end=\"1364\"\u003eNext Generation Sequencing (NGS)\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"1cvh18d\" data-start=\"1366\" data-end=\"1389\"\u003eBenefits of Testing\u003c\/h3\u003e\n\u003cul data-start=\"1390\" data-end=\"1537\"\u003e\n\u003cli data-section-id=\"4usjrz\" data-start=\"1390\" data-end=\"1420\"\u003eAccurate molecular diagnosis\u003c\/li\u003e\n\u003cli data-section-id=\"1w8chyh\" data-start=\"1421\" data-end=\"1462\"\u003eEarly detection of inherited conditions\u003c\/li\u003e\n\u003cli data-section-id=\"bf9p2c\" data-start=\"1463\" data-end=\"1491\"\u003eBetter clinical management\u003c\/li\u003e\n\u003cli data-section-id=\"1to6hjc\" data-start=\"1492\" data-end=\"1537\"\u003eHelps assess genetic risk in family members\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"owkoul\" data-start=\"1539\" data-end=\"1558\"\u003eTurnaround Time\u003c\/h3\u003e\n\u003cul data-start=\"1559\" data-end=\"1614\"\u003e\n\u003cli data-section-id=\"1yivjss\" data-start=\"1559\" data-end=\"1614\"\u003eTypically 2–4 weeks depending on laboratory workflow.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"lgtwr4\" data-start=\"1616\" data-end=\"1634\"\u003eImportant Note\u003c\/h3\u003e\n\u003cp data-start=\"1635\" data-end=\"1758\" data-is-last-node=\"\" data-is-only-node=\"\"\u003eGenetic counseling is recommended before and after testing for proper interpretation of results and family risk evaluation.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"z-0 flex min-h-[46px] justify-start\"\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv class=\"mt-3 w-full empty:hidden\"\u003e\n\u003cdiv class=\"text-center\"\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/section\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"Lifecell Diagnostics","offers":[{"title":"Default Title","offer_id":44007232831623,"sku":null,"price":10010.0,"currency_code":"INR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0691\/4241\/3447\/files\/352372aa-ed93-41f7-baee-a40caf8ba560.png?v=1779525457","url":"https:\/\/ourdermastore.com\/products\/congenital-afibrinogenemia-gene-panel","provider":"Ourdermastore ","version":"1.0","type":"link"}