{"id":12256,"date":"2022-05-26T16:34:00","date_gmt":"2022-05-26T11:04:00","guid":{"rendered":"https:\/\/www.wockhardthospitals.com\/?p=9093"},"modified":"2022-05-26T16:34:00","modified_gmt":"2022-05-26T11:04:00","slug":"man-born-without-a-jaw-on-living-with-otofocial-syndrome-know-about-the-rare-genetic-condition","status":"publish","type":"post","link":"https:\/\/wockhardthospitals.com\/international-patients\/general-health\/man-born-without-a-jaw-on-living-with-otofocial-syndrome-know-about-the-rare-genetic-condition\/","title":{"rendered":"Man Born without a Jaw on Living with Otofocial Syndrome"},"content":{"rendered":"\n<p>Born with a rare congenital disorder called Otofocial syndrome&nbsp;Chicago&nbsp;resident Joseph Williams does not have a jaw. Despite undergoing numerous surgeries, experts have not been able to construct a jaw as his \u201cbody rejected it\u201d, according to various reports.<\/p>\n\n\n\n<p>Due to the condition, he is unable to speak or eat using his mouth. He uses sign language to communicate and eats through a tube.<\/p>\n\n\n\n<p>Sharing his life experiences with&nbsp;<em>Caters News Agency<\/em>, William revealed how people treat him differently due to his&nbsp;medical condition, reported&nbsp;<em>New York Post<\/em>. But he always kept his spirits high by telling himself that \u201cthere is a reason that God made me like this\u201d.<\/p>\n\n\n\n<p>The 41-year-old also opened up about finding love in his wife Vania who he met in 2019, as he said: \u201cWe were friends at first, but we eventually started dating and fell in love. We got married in 2020. I\u2019m sure people would never have expected me to get married. To be honest, I didn\u2019t think I would either.\u201d<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Here\u2019s all you Need to Know About the Medical Condition.<\/h2>\n\n\n\n<p>According to&nbsp;<em>rarediseases.org<\/em>, it is a&nbsp;condition&nbsp;in which a child is without a mandible, and, consequently, without a chin.<\/p>\n\n\n\n<p>\u201cThis disorder affects the development of one\u2019s mouth and is present at birth itself. The symptoms can persist and worsen as one ages,\u201d said Dr. ChandraVeer Singh, consultant otorhinolaryngologist, Head and Neck Onco Surgeon, Wockhardt Hospitals Mira Road.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Causes<\/h2>\n\n\n\n<p>This condition happens due to a mutated gene, said Dr. Singh.<\/p>\n\n\n\n<p>\u201cIn a person with this condition, the&nbsp;tongue&nbsp;will be underdeveloped, making swallowing impossible. Survival becomes challenging, too. It can take a toll on one\u2019s physical and mental well-being. One will have to use sign language or write notes to communicate. Those with this condition require life-long tubal feeding,\u201d said Dr. Singh.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Treatment<\/h2>\n\n\n\n<p>Treatment can include reconstructive surgery for facial clefts, removal of extra teeth, and surgery to repair fused fingers or digit anomalies. It can also include treatment of renal disease including hemodialysis\/peritoneal dialysis or a&nbsp;kidney transplant, explained Dr. Shishir Aggarwal.<\/p>\n\n\n\n<p>\u201cManagement of seizures, if present, and evaluations for learning disabilities may be required based on the type of the syndrome. Speech therapy and special education are also recommended. Other treatment is supportive and based on symptoms,\u201d said Dr. Aggarwal.<\/p>\n\n\n\n<p>Agreed Dr. Singh and added that people with this syndrome need to be monitored closely. \u201cThe treatment for this syndrome will be surgery. So, one will have to follow the guidelines given by the doctor.\u201d<\/p>\n\n\n\n<p><strong><a href=\"https:\/\/www.wockhardthospitals.com\/doctor\/dr-chandra-veer-singh\/\" target=\"_blank\" rel=\"noreferrer noopener\">Dr. ChandraVeer Singh<\/a><br>Consultant Otorhinolaryngologist, Head and Neck Onco Surgeon<br>Wockhardt Hospitals Mira Road<\/strong><\/p>\n\n\n\n<p>To book an appointment call:&nbsp;<a href=\"tel:+918108101104\">+918108101104<\/a><\/p>\n\n\n\n<p>Source: https:\/\/indianexpress.com\/article\/lifestyle\/health\/chicago-man-without-jaw-otoficial-syndrome-rare-genetic-symptoms-treatment-causes-7933146\/<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Born with a rare congenital disorder called Otofocial syndrome&nbsp;Chicago&nbsp;resident Joseph Williams does not have a jaw. Despite undergoing numerous surgeries, experts have not been able to construct a jaw as his \u201cbody rejected it\u201d, according to various reports. Due to the condition, he is unable to speak or eat using his mouth. He uses sign <\/p>\n","protected":false},"author":2,"featured_media":51309,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[97],"tags":[],"class_list":["post-12256","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-general-health"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Man Born without a Jaw on Living with Otofocial Syndrome | Wockhardt Hospitals<\/title>\n<meta name=\"description\" content=\"Born with a rare congenital disorder called Otofocial syndrome Chicago resident Joseph Williams does not have a jaw. 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