Abstract

STUDY DESIGN
Descriptive Observational
PURPOSE
To report a unique case of Fuch’s heterochromic iridocyclitis (FHI), in a rare patient with Klippel Feil Syndrome(KFS)
METHOD
A 41 year old man presented with Left eye(LE) diminution of vision for 6 months and prominent congenital defects.
On slit lamp examination, LE fine stellate keratic precipitates with iris hypochromic heterochromia and a soft white cataract was seen with neovascularisation of the angles on Gonioscopy.
On general examination a short stature, short neck, low hairline, limited range of neck movement, raised right shoulder blade, and long slender finger like thumbs were noted.
X-ray C-spine also revealed C4,5,6 block vertebral formation.

RESULT
This is a typical case of FHI in an atypical case of KFS associated with Sprengel’s deformity, Scoliosis and Triphalangeal thumb
CONCLUSION
FHI has shown association with TORCH infections, Sarcoidosis, Horner’s syndrome, Usher’s syndrome etc. KFS could also be an association