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62 Possible Causes for Macular Heterotopia

  • Generalized Epilepsy with Febrile Seizures Plus

    Show all 6 GPR68 G protein-coupled receptor 68 14q32.11 Ovarian Cancer GPR75 G protein-coupled receptor 75 2p16.2 Age Related Macular Degeneration GPR78 G protein-coupled[genecards.weizmann.ac.il] Bilateral Frontoparietal Polymicrogyria, Polymicrogyria, Bilateral Perisylvian Polymicrogyria, Lennox-Gastaut Syndrome, Neuronal Migration Disorders Periventricular Nodular Heterotopia[genecards.weizmann.ac.il]

  • MELAS Syndrome

    […] degeneration黄斑変性症 macular detachment黄斑剥離 macular edema黄斑浮腫 macular heterotopia黄斑偏位 macular hole黄斑円孔 maculopathy黄斑症 maggotウジ maggot debridement therapy医療用ウジ療法 maggot debridement[jds.or.jp] […] macrophage大食細胞 macrophageマクロファージ macrophage foam-cell formationマクロファージ泡沫細胞形成 macrosomia在胎期間過重量児 macrosomia在胎期間過大児 macrovascular complication大血管合併症 macrovascular disease大血管疾患 macular[jds.or.jp]

  • Schwartz-Jampel Syndrome

    Calmettes 8 reported patients with macular heterotopia associated with blepharophimosis.[doi.org]

  • Retinopathy

    heterotopia or ectopia) ( Figure 16 ).[doi.org] […] distortions of foveal architecture to severe displacements of major retinal vessels, usually temporally and often accompanied by dragging of the retina over the optic disc (macular[doi.org]

  • Hirschsprung Disease Type D-Brachydactyly Syndrome

    , Type I Liver Glycogenosis, Type II Lujan-Fryns Syndrome Lymphangioleiomyomatosis Lymphoedema, Hereditary Lymphoedema-distichiasis Syndrome Macrocephaly/Autism Syndrome Macular[sequencing.com] Syndrome Li-Fraumeni Syndrome Lipodystrophy with Diabetes Lipodystrophy, Familial Partial, Type II (Dunnigan) Lipoprotein Lipase Deficiency Lissencephaly, Subcortical Laminar Heterotopia[sequencing.com]

  • Tubular Aggregate Myopathy

    […] degeneration黄斑変性症 macular detachment黄斑剥離 macular edema黄斑浮腫 macular heterotopia黄斑偏位 macular hole黄斑円孔 maculopathy黄斑症 maggotウジ maggot debridement therapy医療用ウジ療法 maggot debridement[jds.or.jp] […] macrophage大食細胞 macrophageマクロファージ macrophage foam-cell formationマクロファージ泡沫細胞形成 macrosomia在胎期間過重量児 macrosomia在胎期間過大児 macrovascular complication大血管合併症 macrovascular disease大血管疾患 macular[jds.or.jp]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    , Type I Liver Glycogenosis, Type II Lujan-Fryns Syndrome Lymphangioleiomyomatosis Lymphoedema, Hereditary Lymphoedema-distichiasis Syndrome Macrocephaly/Autism Syndrome Macular[sequencing.com] Syndrome Li-Fraumeni Syndrome Lipodystrophy with Diabetes Lipodystrophy, Familial Partial, Type II (Dunnigan) Lipoprotein Lipase Deficiency Lissencephaly, Subcortical Laminar Heterotopia[sequencing.com]

  • Familial Infantile Bilateral Striatal Necrosis

    , Type I Liver Glycogenosis, Type II Lujan-Fryns Syndrome Lymphangioleiomyomatosis Lymphoedema, Hereditary Lymphoedema-distichiasis Syndrome Macrocephaly/Autism Syndrome Macular[sequencing.com] Syndrome Li-Fraumeni Syndrome Lipodystrophy with Diabetes Lipodystrophy, Familial Partial, Type II (Dunnigan) Lipoprotein Lipase Deficiency Lissencephaly, Subcortical Laminar Heterotopia[sequencing.com]

  • Congenital Alpha-2-Antiplasmin Deficiency

    , Type I Liver Glycogenosis, Type II Lujan-Fryns Syndrome Lymphangioleiomyomatosis Lymphoedema, Hereditary Lymphoedema-distichiasis Syndrome Macrocephaly/Autism Syndrome Macular[sequencing.com] Syndrome Li-Fraumeni Syndrome Lipodystrophy with Diabetes Lipodystrophy, Familial Partial, Type II (Dunnigan) Lipoprotein Lipase Deficiency Lissencephaly, Subcortical Laminar Heterotopia[sequencing.com]

  • Retinopathy of Prematurity

    heterotopia or ectopia) ( Figure 16 ).[doi.org] […] distortions of foveal architecture to severe displacements of major retinal vessels, usually temporally and often accompanied by dragging of the retina over the optic disc (macular[doi.org]

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