{"id":2263,"date":"2025-06-27T06:05:49","date_gmt":"2025-06-27T06:05:49","guid":{"rendered":"https:\/\/www.drpectus.com\/conditions-accompanied-by-various-syndromes\/"},"modified":"2025-11-06T17:34:37","modified_gmt":"2025-11-06T17:34:37","slug":"conditions-accompanied-by-various-syndromes","status":"publish","type":"page","link":"https:\/\/www.drpectus.com\/tr\/conditions-accompanied-by-various-syndromes\/","title":{"rendered":"\u00c7e\u015fitli Sendromlarla Birlikte G\u00f6r\u00fclen Durumlar"},"content":{"rendered":"[vc_row type=”in_container” full_screen_row_position=”middle” column_margin=”default” column_direction=”default” column_direction_tablet=”default” column_direction_phone=”default” scene_position=”center” text_color=”dark” text_align=”left” row_border_radius=”none” row_border_radius_applies=”bg” overflow=”visible” overlay_strength=”0.3″ gradient_direction=”left_to_right” shape_divider_position=”bottom” bg_image_animation=”none”][vc_column column_padding=”no-extra-padding” column_padding_tablet=”inherit” column_padding_phone=”inherit” column_padding_position=”all” column_element_direction_desktop=”default” column_element_spacing=”default” desktop_text_alignment=”center” tablet_text_alignment=”default” phone_text_alignment=”default” background_color_opacity=”1″ background_hover_color_opacity=”1″ column_backdrop_filter=”none” column_shadow=”none” column_border_radius=”none” column_link_target=”_self” column_position=”default” gradient_direction=”left_to_right” overlay_strength=”0.3″ width=”1\/1″ tablet_width_inherit=”default” animation_type=”default” bg_image_animation=”none” border_type=”simple” column_border_width=”none” column_border_style=”solid” column_padding_type=”default” gradient_type=”default”][image_with_animation image_url=”1583″ image_size=”full” max_width=”100%” max_width_mobile=”default” animation_type=”entrance” animation=”None” animation_movement_type=”transform_y” hover_animation=”none” alignment=”” border_radius=”none” box_shadow=”none” image_loading=”default”][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n
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Akhondroplazi<\/strong><\/p>\n

Akhondroplazi, genetik ge\u00e7i\u015fli bir k\u0131k\u0131rdak geli\u015fim bozuklu\u011fudur.<\/strong>
Bu durum, g\u00f6\u011f\u00fcs kafesinde %35\u201353 oran\u0131nda daralmaya<\/strong> neden olur.
Ortalama boydaki bireylerle kar\u015f\u0131la\u015ft\u0131r\u0131ld\u0131\u011f\u0131nda, g\u00f6\u011f\u00fcs \u00e7evresi %25\u201330 oran\u0131nda k\u00fc\u00e7\u00fclm\u00fc\u015ft\u00fcr.<\/strong><\/p>\n

\u00d6zellikle erkeklerde, g\u00f6\u011f\u00fcs kafesinin yatay \u00e7ap\u0131 normale yak\u0131n<\/strong> olsa da, \u00f6n-arka (antero-posterior) \u00e7ap\u0131 belirgin \u015fekilde daha k\u00fc\u00e7\u00fckt\u00fcr.<\/strong><\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Anterior Torasik Displazi<\/strong><\/p>\n

Poland sendromunda oldu\u011fu gibi, etkilenen tarafta meme dokusunun geli\u015fmemesi veya yoklu\u011fu<\/strong> ile birlikte g\u00f6\u011f\u00fcs duvar\u0131ndaki yap\u0131lar\u0131n geli\u015fim eksikli\u011fi veya yoklu\u011fu<\/strong> g\u00f6r\u00fcl\u00fcr.
Ancak Poland sendromundan farkl\u0131 olarak<\/strong>, bu durumda pektoral kas\u0131n yoklu\u011fu g\u00f6zlenmez.<\/strong><\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Noonan Sendromu<\/strong><\/p>\n

Noonan Sendromu, k\u0131sa boy<\/strong> ve do\u011fu\u015ftan kalp hastal\u0131\u011f\u0131<\/strong> ile karakterize, genetik ge\u00e7i\u015fli<\/strong> bir hastal\u0131kt\u0131r.
Hem erkeklerde hem kad\u0131nlarda e\u015fit oranda<\/strong> g\u00f6r\u00fcl\u00fcr ve bir\u00e7ok organ\u0131 etkileyen<\/strong> bile\u015fenleri vard\u0131r.
\u0130skelet sistemiyle ilgili bile\u015fenleri aras\u0131nda g\u00f6\u011f\u00fcs duvar\u0131 deformiteleri<\/strong> ve pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> bulunur.<\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Marfan Sendromu<\/strong><\/p>\n

Marfan Sendromu, genetik ge\u00e7i\u015fli<\/strong> bir hastal\u0131kt\u0131r.
Bazen yaln\u0131zca belirli belirtilerle ortaya \u00e7\u0131kabilirken, baz\u0131 durumlarda yenido\u011fan d\u00f6neminden itibaren bir\u00e7ok sistemi etkileyebilecek kadar \u00e7ok say\u0131da bile\u015fen<\/strong> g\u00f6sterebilir.<\/p>\n

En s\u0131k olarak g\u00f6z, kalp ve kas-iskelet sistemi anomalileri<\/strong> ile kendini g\u00f6sterir, ancak di\u011fer organlar\u0131 da etkileyebilir.<\/strong>
\u0130skelet sistemi anomalileri aras\u0131nda g\u00f6\u011f\u00fcs kafesi deformiteleri<\/strong> de yer al\u0131r.
Pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong>, Marfan sendromu tan\u0131s\u0131nda kullan\u0131lan kriterlerde bir puan de\u011ferinde<\/strong> bir bulgu olarak kabul edilir.<\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Osteogenezis \u0130mperfekta<\/strong><\/p>\n

Halk aras\u0131nda \u201ccam kemik hastal\u0131\u011f\u0131\u201d<\/strong> olarak da bilinen bu genetik hastal\u0131kta, kemiklerin \u00e7ok kolay k\u0131r\u0131labilir<\/strong> olmas\u0131 s\u00f6z konusudur.
Bu durum, Tip 1 kollajen \u00fcretimindeki bir bozukluktan<\/strong> kaynaklan\u0131r.
Nadir g\u00f6r\u00fclmekle birlikte, literat\u00fcrde g\u00f6\u011f\u00fcs duvar\u0131 kemiklerini de etkileyebildi\u011fi<\/strong> bildirilmi\u015ftir.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

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Ehlers-Danlos Sendromu<\/strong><\/p>\n

Ehlers-Danlos Sendromu da kal\u0131tsal (genetik ge\u00e7i\u015fli)<\/strong> bir hastal\u0131kt\u0131r.
V\u00fccudun dolgu dokusu olarak g\u00f6rev yapan ba\u011f dokusundaki yap\u0131sal bir bozukluktan<\/strong> kaynaklan\u0131r.
Bu nedenle dokularda gev\u015feklik<\/strong> \u00f6n plandad\u0131r ve cilt, eklemler ve kan damarlar\u0131nda<\/strong> \u00e7e\u015fitli problemler ortaya \u00e7\u0131kabilir.<\/p>\n

A\u015f\u0131r\u0131 esneklik (hipermobilite)<\/strong> bu sendromun tipik \u00f6zelli\u011fidir.
Pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> ise bu sendromun s\u0131k g\u00f6r\u00fclen bile\u015fenlerinden biridir.<\/strong><\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Spinal Musk\u00fcler Atrofi (SMA)<\/strong><\/p>\n

Spinal Musk\u00fcler Atrofi (SMA)<\/strong>, genetik ge\u00e7i\u015fli<\/strong> bir hastal\u0131kt\u0131r.
Sinir sistemini etkiledi\u011fi<\/strong> i\u00e7in kas hareketlerinde bozulmalara yol a\u00e7ar ve ilerleyici<\/strong> bir seyir g\u00f6sterir.
Nadir g\u00f6r\u00fclen bu hastal\u0131kta, t\u00fcm SMA Tip 1<\/strong> hastalar\u0131nda ve baz\u0131 SMA Tip 2<\/strong> hastalar\u0131nda, erken d\u00f6nemde tedavi edilmedikleri takdirde pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> geli\u015febilir.<\/p>\n

Bu durum, diyafram kas\u0131n\u0131n kontrols\u00fcz kas\u0131lmas\u0131<\/strong> sonucu, hastalar\u0131n nefes al\u0131rken g\u00f6\u011f\u00fcs kafesinin d\u0131\u015fa geni\u015flemek yerine i\u00e7e do\u011fru \u00e7\u00f6kmesi<\/strong> nedeniyle ortaya \u00e7\u0131kar.<\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

Loeys-Dietz Sendromu<\/strong><\/p>\n

Loeys-Dietz Sendromu, genetik ge\u00e7i\u015fli<\/strong> bir hastal\u0131kt\u0131r ve \u00e7oklu sistemleri etkileyen karma\u015f\u0131k bir tabloya sahiptir.
Ba\u015fl\u0131ca bulgular\u0131 \u015funlard\u0131r:<\/p>\n

Damar sistemi sorunlar\u0131:<\/strong> Damar duvarlar\u0131nda balonla\u015fma (anevrizma)<\/strong> ve y\u0131rt\u0131lmalar<\/strong> en \u00f6nemli bulgudur. Bu nedenle hastalar yak\u0131n ve d\u00fczenli takip<\/strong> gerektirir.<\/p>\n

\u0130skelet bulgular\u0131:<\/strong> Pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> d\u00e2hil \u00e7e\u015fitli iskelet anomalileri g\u00f6r\u00fclebilir.<\/p>\n

Kafa ve y\u00fcz \u00f6zellikleri:<\/strong> Geni\u015f aral\u0131kl\u0131 g\u00f6zler<\/strong>, \u015fa\u015f\u0131l\u0131k<\/strong>, yar\u0131k damak<\/strong> ve kafatas\u0131nda b\u0131ng\u0131ldaklar\u0131n erken kapanmas\u0131 (kraniosinostoz)<\/strong> s\u0131k g\u00f6r\u00fclen \u00f6zelliklerdir.<\/p>\n

Deri bulgular\u0131:<\/strong> Kadifemsi ve saydam cilt<\/strong>, kolay morarma<\/strong> ve anormal yara izi olu\u015fumu<\/strong> tipiktir.<\/p>\n

Hastal\u0131\u011f\u0131n en ciddi y\u00f6n\u00fc, damarlarda olu\u015fan balonla\u015fmalar (anevrizmalar)<\/strong> oldu\u011fundan, s\u00fcrekli kardiyovask\u00fcler takip<\/strong> hayati \u00f6nem ta\u015f\u0131r.[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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\u00c7\u00f6lyak Hastal\u0131\u011f\u0131<\/strong><\/p>\n

\u00c7\u00f6lyak hastal\u0131\u011f\u0131, bu\u011fday, arpa ve \u00e7avdar gibi tah\u0131llarda bulunan \u201cgluten\u201d adl\u0131 proteine kar\u015f\u0131 alerjik bir reaksiyonun geli\u015fmesi<\/strong> sonucu ortaya \u00e7\u0131kan bir hastal\u0131kt\u0131r. Bu durum, ince ba\u011f\u0131rsa\u011f\u0131n ba\u015flang\u0131\u00e7 k\u0131sm\u0131nda yap\u0131sal de\u011fi\u015fikliklere<\/strong> yol a\u00e7ar. Buna ba\u011fl\u0131 olarak, demir ve folik asit gibi baz\u0131 besin bile\u015fenlerinin ba\u011f\u0131rsaktan kana emilimi bozulur<\/strong> ve bu eksikliklere ba\u011fl\u0131 ek sa\u011fl\u0131k sorunlar\u0131<\/strong> geli\u015febilir.<\/p>\n

Hastal\u0131\u011f\u0131n ailesel ge\u00e7i\u015fi<\/strong> s\u0131k g\u00f6r\u00fclmektedir. Ayr\u0131ca, yap\u0131lan \u00e7al\u0131\u015fmalarda \u00e7\u00f6lyak hastalar\u0131n\u0131n yakla\u015f\u0131k %1\u2019inde a\u00e7\u0131klanamayan bir nedenle pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> e\u015flik etti\u011fi bildirilmi\u015ftir.<\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Charcot-Marie-Tooth Hastal\u0131\u011f\u0131<\/strong><\/p>\n

Charcot-Marie-Tooth hastal\u0131\u011f\u0131, sinir sistemiyle ili\u015fkili<\/strong> genetik bir hastal\u0131kt\u0131r.
Beyin ve omurilik d\u0131\u015f\u0131ndaki periferik sinirlerin hasar g\u00f6rmesi<\/strong> sonucunda, \u00f6zellikle el ve ayak kaslar\u0131nda g\u00fc\u00e7s\u00fczl\u00fck<\/strong> ortaya \u00e7\u0131kar.<\/p>\n

Bu sendromun bile\u015fenlerinden biri de pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> veya di\u011fer g\u00f6\u011f\u00fcs duvar\u0131 deformiteleri<\/strong> olabilir ve bu durum hastal\u0131\u011fa e\u015flik edebilir.<\/strong><\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Atelosteogenezis Sendromlar\u0131<\/strong><\/p>\n

Atelosteogenezis Sendromlar\u0131, birden fazla tipi bulunan<\/strong> genetik k\u00f6kenli bir hastal\u0131k grubudur.
Bu sendromlar\u0131n ortak \u00f6zelli\u011fi, v\u00fccutta kemik geli\u015fimiyle ilgili bozukluklar\u0131n bulunmas\u0131d\u0131r.<\/strong><\/p>\n

Etkilenen bireyler genellikle i\u00e7e ve yukar\u0131 d\u00f6n\u00fck ayaklar (\u00e7arp\u0131k ayak \u2013 clubfoot)<\/strong> ile do\u011farlar ve kal\u00e7a, diz ve dirsek eklemlerinde \u00e7\u0131k\u0131klar<\/strong> g\u00f6r\u00fcl\u00fcr.
Omurga, g\u00f6\u011f\u00fcs kafesi, le\u011fen kemi\u011fi ve uzuvlardaki kemikler<\/strong> geli\u015fmemi\u015f olabilir veya baz\u0131 durumlarda tamamen yok<\/strong> olabilir.<\/p>\n

Bu kemik geli\u015fim bozukluklar\u0131 sonucunda, bireylerde \u00e7ok k\u0131sa kollar ve bacaklar<\/strong> g\u00f6r\u00fcl\u00fcr.
Ayr\u0131ca, iman tahtas\u0131 (sternum) kemi\u011fi<\/strong> de d\u00e2hil olmak \u00fczere t\u00fcm kemiklerin etkilenmesi nedeniyle \u00e7e\u015fitli g\u00f6\u011f\u00fcs duvar\u0131 deformiteleri<\/strong> ve pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> da tabloya e\u015flik edebilir.<\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Pierre-Robin Sendromu<\/strong><\/p>\n

Pierre-Robin Sendromu\u2019nun temel olarak \u00fc\u00e7 ana bile\u015feni<\/strong> vard\u0131r:
Alt \u00e7enenin (mandibula) yeterince geli\u015fmemesi sonucu yar\u0131k damak olu\u015fumu<\/strong>, dilin geriye do\u011fru yerle\u015fmesi (glossopitozis)<\/strong> ve damak kemiklerinin kayna\u015fmamas\u0131<\/strong>.<\/p>\n

Bunlara ek olarak, pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong>, kaburga anomalileri<\/strong> ve k\u00fcrek kemi\u011finin (skapula) alt u\u00e7lar\u0131n\u0131n geli\u015fim gerili\u011fi<\/strong> de sendromda s\u0131k g\u00f6r\u00fclen di\u011fer bulgulard\u0131r.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/article>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Sotos Sendromu<\/strong><\/p>\n

Sotos Sendromu, kemiklerin a\u015f\u0131r\u0131 b\u00fcy\u00fcmesiyle karakterize<\/strong> genetik bir hastal\u0131kt\u0131r.
Do\u011fumda v\u00fccut a\u011f\u0131rl\u0131\u011f\u0131 ve boy uzunlu\u011fu y\u00fcksektir.<\/strong> Kollar ve bacaklar uzun, el ve ayaklar b\u00fcy\u00fck<\/strong> yap\u0131dad\u0131r.
Uzun ve dar y\u00fcz \u015fekli<\/strong> ile yanaklarda k\u0131zar\u0131kl\u0131k<\/strong> sendromun tipik \u00f6zelliklerindendir.
Kafatas\u0131 (kranium)<\/strong> normalden belirgin \u015fekilde b\u00fcy\u00fckt\u00fcr.<\/p>\n

Bunlar\u0131n yan\u0131 s\u0131ra, kalp-damar sistemi<\/strong>, idrar yollar\u0131<\/strong> ve omurga anomalileri<\/strong> s\u0131k g\u00f6r\u00fcl\u00fcr.
Beyin geli\u015fimi yetersiz<\/strong> olabilir ve buna ba\u011fl\u0131 olarak \u00f6\u011frenme g\u00fc\u00e7l\u00fc\u011f\u00fc<\/strong> veya zihinsel gerilik<\/strong> e\u015flik edebilir.
Ayr\u0131ca, kemiklerdeki a\u015f\u0131r\u0131 b\u00fcy\u00fcme<\/strong> nedeniyle g\u00f6\u011f\u00fcs duvar\u0131 deformiteleri<\/strong> de tabloya e\u015flik edebilir.<\/p>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Sprengel Deformitesi<\/strong><\/p>\n

Sprengel Deformitesi, k\u00fcrek kemi\u011finin (skapula) do\u011fu\u015ftan yukar\u0131da yerle\u015fmi\u015f olmas\u0131<\/strong> durumudur.
Bu deformite s\u0131kl\u0131kla di\u011fer kemik patolojileriyle birlikte<\/strong> g\u00f6r\u00fcl\u00fcr.
E\u015flik edebilen durumlar aras\u0131nda g\u00f6\u011f\u00fcs kafesi deformiteleri<\/strong> ve pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> da yer al\u0131r.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Radyal Kl\u00fcp Sendromu ve Holt-Oram Sendromu<\/strong><\/p>\n

Radyal Kl\u00fcp Sendromu<\/strong>, \u00f6n kolun ana kemiklerinden biri olan radius kemi\u011finin geli\u015fim gerili\u011fi<\/strong> ile karakterizedir.
Bu durumda, el bilekten itibaren ba\u015fparmak y\u00f6n\u00fcne do\u011fru e\u011filmi\u015f<\/strong> \u015fekilde durur. Ba\u015fparmak eksik<\/strong> olabilir veya geli\u015fmemi\u015f (hipoplastik)<\/strong> olabilir.<\/p>\n

Bu tablo tek ba\u015f\u0131na<\/strong> g\u00f6r\u00fclebilece\u011fi gibi, \u00e7e\u015fitli genetik sendromlar\u0131n bir par\u00e7as\u0131<\/strong> olarak da ortaya \u00e7\u0131kabilir.
Literat\u00fcrde, radyal kl\u00fcp deformitesinin Holt-Oram Sendromu\u2019nun bir bile\u015feni olarak g\u00f6r\u00fcld\u00fc\u011f\u00fc durumlarda<\/strong>, pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> gibi g\u00f6\u011f\u00fcs duvar\u0131 deformitelerinin<\/strong> de e\u015flik edebildi\u011fi<\/strong> bildirilmi\u015ftir.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n[\/vc_column_text][vc_column_text css=”” text_direction=”default”]\"\"<\/p>\n

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Jarcho-Levin Sendromu<\/strong><\/p>\n

Jarcho-Levin Sendromu\u2019nda, kaburgalar\u0131n omurga ile birle\u015fiminde yap\u0131sal bir bozukluk<\/strong> bulunur.
Kaburgalar birbirleriyle kayna\u015fm\u0131\u015f (f\u00fczyon halinde)<\/strong> olabilir ve bu durum g\u00f6\u011f\u00fcs kafesine \u201cyenge\u00e7 benzeri\u201d bir g\u00f6r\u00fcn\u00fcm<\/strong> kazand\u0131r\u0131r.<\/p>\n

Ayr\u0131ca, omurga anomalilerine ba\u011fl\u0131 olarak sinir sistemi bozukluklar\u0131<\/strong> da g\u00f6r\u00fclebilir.
Kaburga anormalliklerine<\/strong> ba\u011fl\u0131 olarak g\u00f6\u011f\u00fcs duvar\u0131 deformiteleri<\/strong> ve pektus ekskavatum (g\u00f6\u011f\u00fcs \u00e7\u00f6k\u00fckl\u00fc\u011f\u00fc)<\/strong> da tabloya e\u015flik edebilir.<\/strong><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n[\/vc_column_text][\/vc_column][\/vc_row][vc_row type=”in_container” full_screen_row_position=”middle” column_margin=”default” column_direction=”default” column_direction_tablet=”default” column_direction_phone=”default” scene_position=”center” text_color=”dark” text_align=”left” row_border_radius=”none” row_border_radius_applies=”bg” overflow=”visible” overlay_strength=”0.3″ gradient_direction=”left_to_right” shape_divider_position=”bottom” bg_image_animation=”none”][vc_column column_padding=”no-extra-padding” column_padding_tablet=”inherit” column_padding_phone=”inherit” column_padding_position=”all” column_element_direction_desktop=”default” column_element_spacing=”default” desktop_text_alignment=”default” tablet_text_alignment=”default” phone_text_alignment=”default” background_color_opacity=”1″ background_hover_color_opacity=”1″ column_backdrop_filter=”none” column_shadow=”none” column_border_radius=”none” column_link_target=”_self” column_position=”default” gradient_direction=”left_to_right” overlay_strength=”0.3″ width=”1\/1″ tablet_width_inherit=”default” animation_type=”default” bg_image_animation=”none” border_type=”simple” column_border_width=”none” column_border_style=”solid”][\/vc_column][\/vc_row]\n","protected":false},"excerpt":{"rendered":"

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