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909 Possible Causes for Cerebellar Signs during Episodes, Microphthalmos

  • Meckel Syndrome

    Cryptophthalmos, clinical anophthalmia, and microphthalmos with sclerocornea and microcornea have been reported.[disorders.eyes.arizona.edu] sign , hypotonia , developmental delay .[bredagenetics.com] M Warburg, Classification of microphthalmos and coloboma., Journal of Medical Genetics, 10.1136/jmg.30.8.664, 30, 8, (664-669), (1993). H.M. Ramadani and H.A.[doi.org]

  • Micturition Syncope

    • Forty patients were diagnosed as having complex microphthalmos on the basis of a malformed globe with a total axial length measurement at least 2 SDs below the mean for[jamanetwork.com] Microphthalmos, right eye.[eyewiki.aao.org] Measurements of total axial length indicated that complex microphthalmos was congenital and that postnatal growth of the malformed eye was similar to that of normal eyes.[jamanetwork.com]

    Missing: Cerebellar Signs during Episodes
  • Hallermann-Streiff Syndrome

    The microphthalmos had overlapping posterior segment findings usually reported with Nanophthalmos and Posterior microphthalmos.[ncbi.nlm.nih.gov] All patients had a microcornea and microphthalmos. Three patients had a membranous cataract.[ncbi.nlm.nih.gov] Typical features of this syndrome include microphthalmos, proportionate dwarfism, dyscephaly with birdlike facies, dental abnormalities, and hypotrichosis.[ncbi.nlm.nih.gov]

    Missing: Cerebellar Signs during Episodes
  • Patau Syndrome

    Please log in to edit this article. Edit Synonym: Trisomy 13, Bartholin-Patau-Syndrome German : Trisomie 13, Pätau-Syndrom 1 Definition The Patau syndrome, also known as trisomy 13, is a malformation syndrome that is caused by a numerical chromosome aberration. A separation error during the meiosis leads to there[…][flexikon.doccheck.com]

    Missing: Cerebellar Signs during Episodes
  • Congenital Muscular Dystrophy

    […] abnormalities such as crossed eyes (strabismus), cataracts, nearsightedness (myopia), abnormal eye movements, and, in severe cases, retinal detachment and abnormally small eyes (microphthalmos[rarediseases.org] […] detachment have been reported in a high number of patients accompanied or not by other ophthalmological alterations such as abnormal eye movements, strabismus, myopia and microphthalmos[doi.org]

    Missing: Cerebellar Signs during Episodes
  • Microangiopathy

    • Forty patients were diagnosed as having complex microphthalmos on the basis of a malformed globe with a total axial length measurement at least 2 SDs below the mean for[jamanetwork.com] Posterior segment changes associated with posterior microphthalmos.[tandfonline.com] Microphthalmos, right eye.[eyewiki.aao.org]

    Missing: Cerebellar Signs during Episodes
  • Fraser Syndrome

    Computerized Tomography revealed left microphthalmos and a malformation like-coloboma into right ocular globe with cysts and a small calcification parietal anterior.[ncbi.nlm.nih.gov] It was revealed also high-grade microphthalmos in the left ocular globe with persistent primary vitreous and retinal detachment distal.[ijponline.biomedcentral.com] […] sternum [ more ] 0006714 Aplasia/Hypoplasia of the thumb Absent/small thumb Absent/underdeveloped thumb [ more ] 0009601 Autosomal recessive inheritance 0000007 Bilateral microphthalmos[rarediseases.info.nih.gov]

    Missing: Cerebellar Signs during Episodes
  • Mesenteric Infarction

    • Forty patients were diagnosed as having complex microphthalmos on the basis of a malformed globe with a total axial length measurement at least 2 SDs below the mean for[jamanetwork.com] Microphthalmos, right eye.[eyewiki.aao.org] Measurements of total axial length indicated that complex microphthalmos was congenital and that postnatal growth of the malformed eye was similar to that of normal eyes.[jamanetwork.com]

    Missing: Cerebellar Signs during Episodes
  • Laurence Moon Syndrome

    […] disabilities) 759.89 Marchesani (-Weill) syndrome (brachymorphism and ectopia lentis) 759.89 Meyer-Schwickerath and Weyers syndrome (dysplasia oculodentodigitalis) 759.89 Microphthalmos[icd9data.com] […] intellectual disabilities) 759.89 Marchesani (-Weill) (brachymorphism and ectopia lentis) 759.89 Menkes' 759.89 Meyer-Schwickerath and Weyers (dysplasia oculodentodigitalis) 759.89 microphthalmos[icd9data.com]

    Missing: Cerebellar Signs during Episodes
  • Pierre Robin Syndrome

    Summary Epidemiology The prevalence of this syndrome has been estimated at 1 in 10 000 births, but precise values are difficult to obtain because the definition of the syndrome is variable, with some studies including cases were Pierre-Robin sequence occurs as part of a recognised syndrome. Clinical description This[…][orpha.net]

    Missing: Cerebellar Signs during Episodes

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