-
Sclerocornea is an
extremely rare
congenital anomaly of the eye, it is
considered a form of
congenital corneal opacity (CCO) with no
clear gender bias...
- Microphthalmia–dermal aplasia–
sclerocornea syndrome is a
condition characterized by
linear skin lesions. MLS is a rare X-linked
dominant male-lethal disease...
-
following birth trauma.
Causes of
congenital corneal opacities include sclerocornea, trauma, ulcer, mucopolysaccharidosis, Peter’s anomaly,
congenital hereditary...
-
Syndromic microphthalmia is a
class of rare
congenital anomalies characterized by
microphthalmia along with
other non-ocular malformations.
Syndromic microphthalmia...
-
syndrome Lenz
microphthalmia syndrome MCOPS12 Microphthalmia–dermal aplasia–
sclerocornea syndrome Nance–Horan
syndrome Oculofaciocardiodental syndrome Patau syndrome...
-
syndrome Sciatica Scimitar syndrome Scleredema Scleroatonic myopathy Sclerocornea, syndactyly,
ambiguous genitalia Scleroderma Scleromyxedema Sclerosing...
-
Microphthalmia with limb
anomalies Microphthalmos, microcornea, and
sclerocornea Microscopic polyangiitis Microsomia hemifacial radial defects Microspherophakia...
-
Micro syndrome Microdeletion syndrome Microphthalmia–dermal aplasia–
sclerocornea syndrome Middle cerebral artery syndrome Middle child syndrome Middle...
- PAX6 gene mutation. The
aniridic probands showed typical features of
sclerocornea with
nystagmus in
proband 28–1 (A);
Foveal hypoplasia in
proband 27–1...
- McCune–Albright
syndrome McCusick syndrome Metageria Microphthalmia–dermal aplasia–
sclerocornea syndrome Mitis junctional epidermolysis bullosa (nonlethal junctional...
