Syndromic Craniofacial Anomalies
Anomalies of the Craniofacial Structure (Syndromic)
- Crouzon Syndrome – It is considered to be a form of Craniosynostosis. A genetic disorder in which the fibrous joints are closed prematurely. Not allowing the skull to form and take a normal shape.
- Apert Syndrome – A form of deformity of the skull and the face when the sections of the skull bone fuse together prematurely when they are just infants. The regions that effect are skull, eyes, face, palate, hands & feet.
- Treacher Collins Syndrome or Pierre Robin Sequence – A deformity of the lower jaw (abnormally a smaller jaw) often leading to various illness such as difficulty in breathing. In such cases a surgical procedure in extending the lower jaw would solve the illness.
- Hemifacial or Craniofacial Microsomia – A deformity which occurs on one of the sides of the face which also includes the ear and the jaw bone.
- Pierre Robin Syndrome – Also known as Pierre Robin Sequence or Pierre Robin malformation is congenital birth defect which causes backward displacement of jaw, upper airway obstruction or even underdeveloped jaw usually the syndrome is common among twins.
- Cleft Lip & Palate - A deformity which is commonly seen in children where only a partial formation of the lip is developed by birth. A procedure perfected by our elite award-winning surgeons at the best cleft centre in India at Klinik Glühen.
- Vascular Malformations of the face - An abnormality that effect the children and adults which looks like a big mass / lump on the face along with blemishes which may cause pain, swelling or bleeding. It usually occurs due to odd growth to the lymph vessels / arteries or blood vessels. This is seen with abnormal connections between the veins and the arteries as we age and increased blood flow. This is present at birth and progresses as we age.
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