{"id":27135,"date":"2025-06-24T14:44:08","date_gmt":"2025-06-24T12:44:08","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/panel-obezitate-monogenica\/"},"modified":"2026-02-27T17:58:10","modified_gmt":"2026-02-27T15:58:10","slug":"panel-obezitate-monogenica","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-diagnostic-genetic\/panel-obezitate-monogenica\/","title":{"rendered":"Panel Obezitate monogenica"},"content":{"rendered":"<p><strong>Obezitatea monogenic\u0103<\/strong> este o form\u0103 rar\u0103 de obezitate sever\u0103, precoce \u0219i ereditar\u0103, cauzat\u0103 de muta\u021bii \u00eentr-o singur\u0103 gen\u0103 care afecteaz\u0103 reglarea apetitului, metabolismul energetic sau func\u021bia hormonilor hipotalamici \u0219i periferici.<\/p>\n<\/p>\n<p> Acest panel analizeaz\u0103 gene implicate \u00een:<\/p>\n<\/p>\n<ul>\n<li>semnalizarea leptinei \u0219i receptorului leptinei (LEP, LEPR)<\/li>\n<li>sistemul melanocortin (MC3R, MC4R, POMC, PCSK1, MRAP2)<\/li>\n<li>sindroame genetice cu obezitate asociat\u0103 (BBS, ALMS, RAI1, KSR2 etc.)<\/li>\n<\/ul>\n<p><strong>Afec\u021biuni sau simptome asociate<\/strong><\/p>\n<\/p>\n<ul>\n<li>obezitate sever\u0103 \u00eenc\u0103 din copil\u0103rie<\/li>\n<li>apetit crescut (hiperfagie)<\/li>\n<li>dezechilibre hormonale asociate (leptin\u0103, melanocortine, POMC)<\/li>\n<li>caracteristici sindromice: sindrom Bardet-Biedl, Alstr\u00f6m, sindrom Prader-Willi sau alte dismorfii asociate<\/li>\n<li>posibil risc metabolic crescut (diabet, dislipidemie, hipertensiune)<\/li>\n<\/ul>\n<p><strong>Cui se adreseaz\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>copiilor \u0219i adul\u021bilor cu obezitate sever\u0103 precoce (de obicei debut \u00eenainte de 10 ani)<\/li>\n<li>persoanelor cu istoric familial de obezitate monogenic\u0103<\/li>\n<li>clinicienilor specializa\u021bi \u00een endocrinologie, genetic\u0103 medical\u0103 sau pediatrie<\/li>\n<\/ul>\n<p><strong>Metodologie de testare<\/strong><\/p>\n<\/p>\n<ul>\n<li>secven\u021biere NGS a exonilor \u0219i regiunilor critice de reglare<\/li>\n<li>detecteaz\u0103 variante punctiforme, inser\u021bii \u0219i dele\u021bii<\/li>\n<\/ul>\n<p><strong>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>permite diagnostic molecular precoce \u0219i clarificarea cauzelor obezit\u0103\u021bii<\/li>\n<li>ofer\u0103 informa\u021bii pentru consiliere genetic\u0103 familial\u0103<\/li>\n<li>contribuie la personalizarea strategiilor terapeutice \u0219i dietetice<\/li>\n<li>identific\u0103 persoane cu risc pentru complica\u021bii metabolice asociate<\/li>\n<\/ul>\n<p><strong>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/strong><\/p>\n<\/p>\n<ul>\n<li>nu detecteaz\u0103 formele poligenice sau obezitatea dob\u00e2ndit\u0103 prin factori de mediu<\/li>\n<li>variantele de semnifica\u021bie incert\u0103 (VUS) necesit\u0103 reevaluare \u0219i corelare clinic\u0103<\/li>\n<li>nu exclude alte cauze endocrinologice sau metabolice de obezitate<\/li>\n<\/ul>\n<p><strong>Analize asociate recomandate<\/strong><\/p>\n<\/p>\n<ul>\n<li>testare metabolic\u0103 complet\u0103 (glucoz\u0103, insulin\u0103, lipidogram\u0103)<\/li>\n<li>evaluare endocrinologic\u0103<\/li>\n<li>analize genetice suplimentare \u00een cazul caracteristicilor sindromice<\/li>\n<li>consiliere genetic\u0103 pre- \u0219i post-test<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Panelul NGS analizeaz\u0103 simultan 68 de gene implicate \u00een forme monogenice de obezitate.<\/p>\n<p>Testul identific\u0103 variante genetice care pot fi responsabile de obezitatea sever\u0103 precoce, oferind informa\u021bii utile pentru diagnostic, consiliere genetic\u0103 \u0219i management terapeutic individualizat.<\/p>\n<\/p>\n<p><strong>Gene analizate:<\/strong><\/p>\n<\/p>\n<p>ADCY3, AFF4, ALMS1, ARL6, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BDNF, C8orf37, CEP164, CEP19, CEP290, CPE, CREBBP, CUL4B, DYRK1B, EP300, FBN3, GNAS, GPR101, IFT172, IFT27, IFT74, KDM6A, KIDINS220, KIF7, KMT2D, KSR2, LEP, LEPR, LZTFL1, MAGEL2, MC3R, MC4R, MEGF8, MKKS, MKS1, MRAP2, NLGN2, NPY, NR0B2, NTRK2, PCSK1, PHF6, POMC, PPARG, PRMT7, RAB23, RAI1, RPS6KA3, SCLT1, SDCCAG8, SETD2, SH2B1, SIM1, TRAPPC3, TRAPPC9, TRIM32, TTC8, UCP3, VPS13B, WDPCP.<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3166,2876],"product_tag":[],"class_list":["post-27135","product","type-product","status-publish","product_cat-analize","product_cat-diagnostic-genetic","product_cat-serviciu-laborator","first","instock","sale","virtual","purchasable","product-type-simple"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 5.0.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Panelul NGS analizeaz\u0103 simultan 68 de gene implicate 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Pro (AIOSEO) 5.0.0.1\" \/>\n\t\t<meta property=\"og:locale\" content=\"ro_RO\" \/>\n\t\t<meta property=\"og:site_name\" content=\"Clinica Sante - Laborator de Analize Medicale - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:type\" content=\"article\" \/>\n\t\t<meta property=\"og:title\" content=\"Panel Obezitate monogenica - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:description\" content=\"Panelul NGS analizeaz\u0103 simultan 68 de gene implicate \u00een forme monogenice de obezitate.Testul identific\u0103 variante genetice care pot fi responsabile de obezitatea sever\u0103 precoce, oferind informa\u021bii utile pentru diagnostic, consiliere genetic\u0103 \u0219i management terapeutic individualizat.Gene analizate:ADCY3, AFF4, ALMS1, ARL6, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BDNF, C8orf37, CEP164, CEP19, CEP290, CPE, CREBBP, CUL4B, DYRK1B, EP300, FBN3, GNAS, GPR101, IFT172, IFT27, IFT74, KDM6A, 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obezitatea sever\u0103 precoce, oferind informa\u021bii utile pentru diagnostic, consiliere genetic\u0103 \u0219i management terapeutic individualizat.Gene analizate:ADCY3, AFF4, ALMS1, ARL6, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BDNF, C8orf37, CEP164, CEP19, CEP290, CPE, CREBBP, CUL4B, DYRK1B, EP300, FBN3, GNAS, GPR101, IFT172, IFT27, IFT74, KDM6A, KIDINS220, KIF7, KMT2D, KSR2, LEP, LEPR, LZTFL1, MAGEL2, MC3R, MC4R, MEGF8, MKKS, MKS1, MRAP2, NLGN2, NPY, NR0B2, NTRK2, PCSK1, PHF6, POMC, PPARG, PRMT7, RAB23, RAI1, RPS6KA3, SCLT1, SDCCAG8, SETD2, SH2B1, SIM1, TRAPPC3, TRAPPC9, TRIM32, TTC8, UCP3, VPS13B, WDPCP.\" \/>\n\t\t<script type=\"application\/ld+json\" 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