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Article

Spheroidal degeneration in H626R TGFBI variant lattice dystrophy: a multimodality analysis.

Cornea - 1 Jul 2014

Lai Kevin, Reidy Jason, Bert Benjamin, Milman Tatyana

Abstract excerpt

PURPOSE: The aim of this study was to describe clinical, imaging, molecular genetic, histopathologic, immunohistochemical, and ultrastructural characteristics of coexistent amyloid and spheroidal degeneration-type deposits in a family with histidine-626-arginine transforming growth factor beta-induced (H626R TGFBI) variant lattice dystrophy. METHODS: This is a retrospective clinical-pathological and genetic...

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Share to Amyloid
Share to Amyloidosis, Familial
Share to Corneal Dystrophies, Hereditary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Extracellular Matrix Proteins

Share to Multimodal Imaging

Share to Tomography, Optical Coherence

Share to Transforming Growth Factor beta

Source

Identifiers

PMID: 24831201
DOI: 10.1097/ICO.0000000000000140

Genes

TGFBI
CAT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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