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Microphthalmia (Greek: μικρός ... The face reaches 70% of its adult size by roughly 2 years of age, and 90% of its adult size by about 5.5 years of age. [13 ...
Syndromic microphthalmia is a class of rare congenital anomalies characterized by microphthalmia along with other non-ocular malformations. [2] Syndromic microphthalmia accounts for 60 to 80% of all cases of microphthalmia. [ 2 ]
Lenz microphthalmia syndrome is inherited as an X-linked recessive genetic trait and is fully expressed in males only. Females who carry one copy of the disease gene (heterozygotes) may exhibit some of the symptoms associated with the disorder, such as an abnormally small head (microcephaly), short stature, or malformations of the fingers or toes.
Microphthalmia, syndromic 12 (MCOPS12) is an ultra-rare and complex neurological disease. It is caused by a single-point missense mutation in the retinoic acid receptor beta (RARB) gene . The most common disease symptoms are microphthalmia , severe (progressive) movement disorders and intellectual disability . [ 1 ]
Microphthalmia; Microphthalmia, Lentz type; Microphthalmia camptodactyly mental retardation; Microphthalmia cataract; Microphthalmia diaphragmatic hernia Fallot; Microphthalmia mental deficiency; Microphthalmia microtia fetal akinesia; Microphthalmia with limb anomalies; Microphthalmos, microcornea, and sclerocornea; Microscopic polyangiitis
Narrow airways often widen with age and allow for easier breathing. [3] Dental anomalies are also seen, such as abnormally large dental buds and late eruption of deciduous teeth. [6] Development of the eyes is also affected by warfarin. Microphthalmia, telecanthus and strabismus are common signs of fetal
Patau syndrome is a syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome 13.The extra genetic material disrupts normal development, causing multiple and complex organ defects.
Its highly rare in males, but some males were born with it. Teeth with large roots (radiculomegaly), heart defects and small eyes (microphthalmia) are the characteristic triad found in this syndrome. Typical features of the condition include: [citation needed] Face Deep set eyes; Broad nasal tip divided by a cleft; Eyes Microphthalmia (small eyes)