Congenital corneal opacification in De Barsy syndrome

Archives of Ophthalmology

Volumn 119, Issue 2, 2001, Pages 285-288

  Aldave, A J ^a   Eagle R C , Jr ^a   Streeten, B W ^a   Qi, J ^a   Raber, I M ^a  

^a WILLS EYE HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN; ELASTIN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CORNEA OPACITY; CUTIS LAXA; DE BARSY SYNDROME; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; ELECTRON MICROSCOPY; HISTOPATHOLOGY; HUMAN; HYPERREFLEXIA; INFANT; JOINT HYPERMOBILITY; KERATOPLASTY; MALE; MUSCLE HYPOTONIA; PRIORITY JOURNAL; PROGERIA; SHORT STATURE; TREATMENT OUTCOME;

ABNORMALITIES, MULTIPLE; CORNEA; CORNEAL OPACITY; CUTIS LAXA; DIAGNOSIS, DIFFERENTIAL; EYE DISEASES, HEREDITARY; HUMANS; INFANT, NEWBORN; KERATOPLASTY, PENETRATING; MALE; PROGERIA; SYNDROME;

EID: 0035129029     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

1. Dwarfism, oligophrenia and degeneration of the elastic tissue in skin and cornea: A new syndrome?
2. De Barsy syndrome
3. De Barsy-Syndrom: Eine weitere Beobachtung
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5. De Barsy syndrome: Report of a case, literature review, and elastin gene expression studies of the skin
6. De Barsy syndrome: An autosomal recessive, progeroid syndrome
7. Biochemical, morphological and immunological findings in a patient with a cutis laxa-associated inborn disorder (De Barsy syndrome)
8. Augenbefunde beim de Barsy-Syndrom
9. De Barsy-Moens-Dierckx-Syndrom: Beobachtung bei Geschwistern
10. De Barsy-Moens-Dierckx-Syndrom: Ein ungewohnlicher Verlauf bei einem Fruhgeborenen
11. Drthopaedic manifestations in de Barsy syndrome
12. Comeal dystrophy in Cockayne's syndrome
13. Identical male twins and brother with Cockayne syndrome