Lattice corneal dystrophy. Report of an unusual case.

[Case report of Cogan-like dystrophy diagnosed as confirmed type I lattice corneal dystrophy in a 10-year-old child].

Meretoja's Syndrome: Lattice Corneal Dystrophy, Gelsolin Type.

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.

An Unusual Case of Extensive Lattice Degeneration and Retinal Detachment.

Syringocystadenoma papilliferum: report of an unusual case.

Sporotrichosis in an unusual location--Case report.

Periapical actinomycosis. An unusual case report.

An unusual atlanto-axial dislocation. Case report.

Phenotypic Spectrum of Granular Corneal Dystrophy Type II in Two Italian Families Presenting an Unusual Granular Corneal Dystrophy Type I Clinical Appearance.

Development of allele-specific gene-silencing siRNAs for TGFBI Arg124Cys in lattice corneal dystrophy type I.

A case of choledochoduodenal fistula - an unusual case report.

An unusual case of prostate tuberculosis: a case report.

Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II.

An unusual variant of Becker muscular dystrophy.

A Korean patient with lattice corneal dystrophy type IV with Leu527Arg mutation in the TGFBI gene.

Case Report: An Unusual Presentation of an Incomplete Sentence.

Two mutations in the transforming growth factor beta-induced gene associated with familial Lattice corneal dystrophy.

[Stargardt macular dystrophy - case report].

Cephalic Tetanus in an Immunized Teenager: An Unusual Case Report.

An Unusual Triad in Pediatric Neurology: A Case Report on Cerebral Palsy, Epilepsy, and Duchenne Muscular Dystrophy.

[Hydatid cyst of the liver: report of an unusual case].

Horner's syndrome: an unusual complication of thyroidectomy: a case report.

PROPTOSIS-AN UNUSUAL PRESENTATION OF METASTATIC CARCINOMA PANCREAS: Case Report.

An unusual location of gouty panniculitis: A case report.

Suggest Documents

[Case report of Cogan-like dystrophy diagnosed as confirmed type I lattice corneal dystrophy in a 10-year-old child].

Meretoja's Syndrome: Lattice Corneal Dystrophy, Gelsolin Type.

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.

An Unusual Case of Extensive Lattice Degeneration and Retinal Detachment.

Syringocystadenoma papilliferum: report of an unusual case.

Sporotrichosis in an unusual location--Case report.

Periapical actinomycosis. An unusual case report.

An unusual atlanto-axial dislocation. Case report.

Phenotypic Spectrum of Granular Corneal Dystrophy Type II in Two Italian Families Presenting an Unusual Granular Corneal Dystrophy Type I Clinical Appearance.

Development of allele-specific gene-silencing siRNAs for TGFBI Arg124Cys in lattice corneal dystrophy type I.

A case of choledochoduodenal fistula - an unusual case report.

An unusual case of prostate tuberculosis: a case report.

Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II.

An unusual variant of Becker muscular dystrophy.

A Korean patient with lattice corneal dystrophy type IV with Leu527Arg mutation in the TGFBI gene.

Case Report: An Unusual Presentation of an Incomplete Sentence.

Two mutations in the transforming growth factor beta-induced gene associated with familial Lattice corneal dystrophy.

[Stargardt macular dystrophy - case report].

Cephalic Tetanus in an Immunized Teenager: An Unusual Case Report.

An Unusual Triad in Pediatric Neurology: A Case Report on Cerebral Palsy, Epilepsy, and Duchenne Muscular Dystrophy.

[Hydatid cyst of the liver: report of an unusual case].

Horner's syndrome: an unusual complication of thyroidectomy: a case report.

PROPTOSIS-AN UNUSUAL PRESENTATION OF METASTATIC CARCINOMA PANCREAS: Case Report.

An unusual location of gouty panniculitis: A case report.

Lattice corneal dystrophy. Report of an unusual case.

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