Syndromic 4

Condition Goldenhar Syndrome Henifacial Microsomia Goldenhar Syndrome, also known as oculo-auriculo-vertebral spectrum, is a rare congenital disorder characterized by facial and craniofacial abnormalities. It typically involves underdevelopment of the ear, resulting in hearing loss, as well as jaw and facial asymmetry, eye abnormalities, and spinal defects. Hemifacial Microsomia is a condition in which one side … Read more

Syndromic 3

Condition Hallerman-Streiff Syndrome Hallermann-Streiff syndrome (HSS) is a very rare genetic disorder that can include dental abnormalities, hypotrichosis, skin atrophy, proportionate short stature, and ophthalmic features including microphthalmia and congenital bilateral cataracts. Procedure Performed Lefort 1 Osteotomy. Bilateral Total Joint Replacement (TJR). Genioplasty. Genioglossus Advancement. About This Patient The patient was struggling with severe Obstructive … Read more

Syndromic 2

Condition Treacher Collins Syndrome (TCS). Treacher Collins syndrome (TCS) is a rare genetic disorder that tends to involve underdevelopment of the facial skeleton, cheekbones, jaws, palate and mouth which can lead to breathing and eating difficulties. In addition, affected individuals may also have a downward slant of the opening between the upper and lower eyelids … Read more