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Sclerocornea

A congenital anomaly in which a part or the whole of the cornea acquires the characteristics of sclera, resulting in clouding of the cornea. [HPO… 
National Institutes of Health

Related topics

Related topics

9 relations
Aphakia, congenital primaryDiGeorge SyndromeEncephalocraniocutaneous lipomatosisJejunal Atresia with Microcephaly and Ocular Anomalies

Broader (2)

CorneaCorneal Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome…
2004
2004
Phenotypic variation in ophthalmic manifestations of MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea).
wald E, Fauci AS, Isselbacher KJ, Kasper DL, Hauser SL, Longo DL, Jameson JL, eds. Harrison’s Online. Chap 286. Available at… 
Review
1994
Review
1994
Bilateral penetrating keratoplasty for sclerocornea in an infant with monosomy 21. Case report and review of the literature.
An 8-month-old caucasian girl with monosomy 21 and sclerocornea underwent bilateral penetrating keratoplasties. Both light and… 
Review
1993
Review
1993
MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome.
Bilateral microphthalmia with blepharophimosis, linear lesions of dermal aplasia involving the face, and microcephaly were… 
1992
1992
Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects.
We report on an infant girl with congenital erythematous, linear skin lesions on face and neck, bilateral microphthalmia… 
Review
1992
Review
1992
Sclerocornea and interstitial deletion of the short arm of chromosome 6--(46XY del[6] [p22 p24]).
The interstitial deletion of the short arm of chromosome (6)--46 XY del (6) (p22.3 p24) is unrecorded. The ophthalmic findings in… 
1983
1983
Wound healing of grafts in congenitally opaque infant corneas.
1983
1983
[Sclerocornea. Ultrastructural and morphologic study].
A 6 month old white male infant had bilateral congenital diffuse sclerocornea. A penetrating keratoplasty was performed in his… 
1972
1972
Ocular manifestations of the Meckel syndrome.
The Meckel syndrome is a genetically determined (autosomal recessive) disease with major developmental abnormalities incompatible… 
1962
1962
Sclerocornea and associated congenital anomalies.
Sclerocornea has been described most frequently in conjunction with the entity cornea plana, 1-7 but it may also occur as an… 
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