KID syndrome: About a case

[Use of bevacizumab (Avastin) in KID syndrome: case report].

KID syndrome is a congenital ectodermal dysplasia characterized by the association of keratitis, hyperkeratotic skin lesions and neurosensorial hearing loss. Ocular involvement occurs in 95% of patients. Although KID syndrome cutaneous manifestations have been studied in-depth, the treatment and prognosis of ophthalmic impairment have not been described in detail. At present, the treatment of t...

Parry-romberg syndrome: about a case

A six-year-old girl presented with skin lesions on the left cheek at 5 years of age. On examination diffuse sclerosis on the left cheek was noted, hypoplasia of left half of the face and deviation of mouth and lips to left side were noted. Investigations show normal blood counts and rheumatoid factor and antinuclear antibody were negative. CT scan of brain was normal. Fundus examination reveale...

Infectious keratitis in a patient with kid syndrome.

A 36-year-old man diagnosed with Keratitis-IchthyosisDeafness (KID) syndrome who had loss of vision in his right eye. He had been treated with penetrating keratoplasty on four previous occasions (the last time four years earlier) because of ulcers, corneal leucoma and infections caused by Candida albicans and Pseudomonas aeruginosa. The patient is forced to wear permanent contact lenses because...

Cogan’s Syndrome: A Case Report

Sheehan Syndrome: A Case Report

'rwo cases of post-partum amenorrhea with other clinical signs of She1ehan syndrom was studied at the Loghmandoleh Medical Center, National University of Iran.  Clinical diagnosis was confirmed by appro­priate laboratory work -up in the f.irSlt case and the patient was placed on the conventional end orga.n hormon substitutional therapy (Thy­roid -Gonad -Adrenal) and was discharged in good cond...