A 12 year old girl child from the department of Ophthalmology posted for right eye limbal dermoid excision. Opthlamic examination and history revealed bilateral restricted eye movements, limbal dermoids, and decreased vision since birth. Fundus examination showed pathological myopia. There were multiple preauricular appendages in front of both ears. The lateral X-ray of cervical spine showed fused second and third cervical vertebra with loss of intervertebral disc space. Chest X-ray showed scoliosis of Cervico-Thorasic vertebra with convexity to right. Clinical examination of the airway revealed restricted head and neck movements with Mallampatti class II which indicates difficult intubation. The history, clinical examination and radiologic...
Goldenhar Syndrome (GS) is a congenital disorder with male predominance and sporadic occurrence. Var...
Crouzon syndrome is a rare hereditary disorder, characterised by marked craniofacial dysostosis from...
Morquio syndrome (MS) or mucopolysaccharidosis (MPS) type IVA is a progressive lysosomal storage dis...
Goldenhar syndrome, also known as oculoauriculovertebral dysplasia, is a rare congenital condition c...
Goldenhar syndrome is ocular-auriculo-vertebral dysplasia with cardiac, renal, visceral, and facial ...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
A 6-month-old male child presented to Ophthalmology Outpatient Department of our hospital with decr...
Goldenhar syndrome, also known as oculoauriculovertebral dysplasia, is a rare congenital condition c...
This is a report on a case of Goldenhar syndrome. It shows the usual association of auricular append...
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/146550/1/anr300001hh.pd
Abstract: Goldenhar syndrome is a rare disorder characterized by a wide range of congenital malforma...
The present case emphasizes on the increasing difficulty in management of patients with Goldenhar sy...
Goldenhar Syndrome (GS) is a congenital disorder with male predominance and sporadic occurrence. Var...
Crouzon syndrome is a rare hereditary disorder, characterised by marked craniofacial dysostosis from...
Morquio syndrome (MS) or mucopolysaccharidosis (MPS) type IVA is a progressive lysosomal storage dis...
Goldenhar syndrome, also known as oculoauriculovertebral dysplasia, is a rare congenital condition c...
Goldenhar syndrome is ocular-auriculo-vertebral dysplasia with cardiac, renal, visceral, and facial ...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
Goldenhar syndrome is a congenital disorder involving deformities of the face. It usually affects on...
A 6-month-old male child presented to Ophthalmology Outpatient Department of our hospital with decr...
Goldenhar syndrome, also known as oculoauriculovertebral dysplasia, is a rare congenital condition c...
This is a report on a case of Goldenhar syndrome. It shows the usual association of auricular append...
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/146550/1/anr300001hh.pd
Abstract: Goldenhar syndrome is a rare disorder characterized by a wide range of congenital malforma...
The present case emphasizes on the increasing difficulty in management of patients with Goldenhar sy...
Goldenhar Syndrome (GS) is a congenital disorder with male predominance and sporadic occurrence. Var...
Crouzon syndrome is a rare hereditary disorder, characterised by marked craniofacial dysostosis from...
Morquio syndrome (MS) or mucopolysaccharidosis (MPS) type IVA is a progressive lysosomal storage dis...