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60 Possible Causes for Myopia (in Brother

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  • Kyphoscoliosis

    She and one brother had high myopia as well (parameters not reported).[] Joint Laxity, Short Stature, and Myopia Clinical Characteristics Ocular Features: Three of four brothers in one family had high myopia and two had retinal detachments as well[] Systemic Features: In one consanguineous family a brother and sister had multiple large joint dislocations including elbows, hips, knees and ankles.[]

  • High Myopia-Sensorineural Deafness Syndrome

    A brother of the proband, aged 4 years, had had prominence of the knees and ankles as an infant and showed severe myopia with retinal thinning.[]

  • Hereditary Optic Atrophy

    Elizabeth's vision is normal with the exception of myopia. Elizabeth's deceased father was blind. Her mother has normal vision.[] Elizabeth has two brothers, both of whom have normal vision. One of these brothers has two children, a son and a daughter. Both of these children have normal vision.[]

  • Tel Hashomer Camptodactyly Syndrome

    , facial anomalies, joint contractures, and mild scoliosis in a 13-year-old Turkish girl and her 11-year-old brother.[] […] parents suggest autosomal recessive inheritance of a previously apparently undescribed syndrome of camptodactyly, fibrosis of the medial rectus muscle of the eye, severe myopia[]

  • Autosomal Dominant Larsen Syndrome

    Family 2 consisted of three brothers (ages 20, 16 and 7 years) exhibiting hyper-extensibility of large joints, severe myopia and short stature.[] She and one brother had high myopia as well (parameters not reported).[] She had a 2.5-year-old brother with a similar presentation.[]

  • Brachydactyly of Fingers

    , severe developmental delay, and peculiar facial appearance in two brothers: A new syndrome?[] Radiologic Findings in Congenital Onychodysplasia of the Index Finger Red fingers syndrome and recurrent panniculitis in a patient with chronic hepatitis C Short stature, myopia[]

  • Kaufman Oculocerebrofacial Syndrome

    brothers: A new syndrome?[] Sibylla Achermann, Remo Largo, Dieter Kotzot, Mariluce Riegel and Albert Schinzel, Short stature, myopia, severe developmental delay, and peculiar facial appearance in two[]

  • Marchesani-Weill Syndrome

    He had the same characteristic features as his brother and father corresponding to Weill–Marchesani syndrome including severe myopia, microphakia, and joint stiffness.[] We have described four eyes with severe chronic angle closure glaucoma associated with Weill–Marchesani syndrome in two Amish brothers who presented with increasing myopia[] A brother and a sister from a Saudi Arabian family reported by Khan et al. [ 15 ] with a mutation in the ADAMTS17 gene showed high myopia and microspherophakia, but narrow[]

  • Spondyloepiphyseal Dysplasia Congenita

    His past medical history was significant for bilateral hip dysplasia and myopia, for which he wears glasses.[] Family history was significant for a sister who had been diagnosed with arthritis at 12 years of age and a brother who had bilateral hip replacement at 10 years of age.[]

  • Spastic Ataxia with Congenital Miosis

    Ophthalmic examination showed ptosis, slow pupillary reaction, myopia, optic disc pallor, retinal atrophy, and color blindness.[] A brother of the 2 had similar features. In another branch of the family, 3 members had adult onset of progressive ataxia, dysarthria, and poor vision.[]

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