Corneal pathology in microphthalmia with linear skin defects syndrome

Cornea

Volumn 27, Issue 6, 2008, Pages 734-738

  Kapur, Rashmi ^a   Tu, Elmer Y ^a   Toyran, Sami ^a   Shah, Parthiv ^a   Vangveeravong, Sumalee ^a   Lloyd, William C ^b   Edward, Deepak P ^c  

^a UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^b University of Texas Health Science Center   (United States)

^c SUMMA HEALTH SYSTEM   (United States)

Author keywords

MIDAS syndrome; MLS syndrome; Sclerocornea

Indexed keywords

COLLAGEN; COLLAGEN TYPE 3; KERATAN SULFATE;

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; CORNEA; CORNEA DISEASE; CORNEA THICKNESS; DESCEMET MEMBRANE; EYE EXAMINATION; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOPHENOTYPING; INFANT; KERATOPLASTY; MALE; MICROPHTHALMIA; MICROSCOPY; PETERS ANOMALY; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA DETACHMENT; SCLEROCORNEA; SKIN DEFECT; STAINING; VASCULARIZATION; CONGENITAL MALFORMATION; CONGENITAL SKIN DISEASE; CORNEA OPACITY; EXTRACELLULAR MATRIX; FLUORESCENT ANTIBODY TECHNIQUE; GENETICS; METABOLISM; PATHOLOGY; PENETRATING KERATOPLASTY; SCLERA; SYNDROME;

COLLAGEN TYPE III; CORNEA; CORNEAL OPACITY; EXTRACELLULAR MATRIX; FEMALE; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; HUMANS; IMMUNOPHENOTYPING; INFANT; KERATAN SULFATE; KERATOPLASTY, PENETRATING; MALE; MICROPHTHALMOS; SCLERA; SKIN ABNORMALITIES; SYNDROME;

EID: 47949114484     PISSN: 02773740     EISSN: None     Source Type: Journal    
DOI: 10.1097/QAI.0b013e31815b834d     Document Type: Article

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