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608 Possible Causes for Congenital Heart Disease, Microphthalmos, Myopia

  • Pierre Robin Syndrome

    Congenital heart disease occurs in about 20 percent of patients with Pierre Robin syndrome.[ncbi.nlm.nih.gov] If you are wondering how a baby is diagnosed with myopia, you are not alone![raisingarrows.net] There are often signs of congenital heart disease, such as atrial septal defect (ASD), patent ductus arteriosus, ventricular septal defect (VSD).[doi.org]

  • Laurence Moon Syndrome

    Congenital heart disease 10.[en.wikipedia.org] […] disabilities) 759.89 Marchesani (-Weill) syndrome (brachymorphism and ectopia lentis) 759.89 Meyer-Schwickerath and Weyers syndrome (dysplasia oculodentodigitalis) 759.89 Microphthalmos[icd9data.com] Glaucoma • Stargardt’s Syndrome • Retinal Detachment • Optic Neuritis • Diabetic Retinopathy • Retinitis Pigmentosa • Optic Nerve Atrophy • Cataracts • Usher’s Syndrome • Myopia[pinterest.cl]

  • Congenital Muscular Dystrophy

    Other signs and symptoms of Fukuyama congenital muscular dystrophy include impaired vision, other eye abnormalities, and slowly progressive heart problems after age 10.[ghr.nlm.nih.gov] […] 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] Compared to WWS patients, these patients have milder structural brain abnormalities, and eye abnormalities were absent, except for myopia in some cases.[ncbi.nlm.nih.gov]

  • Marchesani-Weill Syndrome

    Retinal vascular tortuosity in the absence of congenital heart disease has been described in one affected individual [ Gallagher et al 2011 ].[ncbi.nlm.nih.gov] […] disabilities) 759.89 Marchesani (-Weill) syndrome (brachymorphism and ectopia lentis) 759.89 Meyer-Schwickerath and Weyers syndrome (dysplasia oculodentodigitalis) 759.89 Microphthalmos[icd9data.com] Abstract Objective: To describe the presenting features of Weill-Marchesani syndrome Case: A 22-year-old man presented with high myopia and progressive visual disturbance.[nepjol.info]

  • Microcornea

    Congenital rubella syndrome was observed in 16 (80%) of the patients with congenital heart disease.[healio.com] PURPOSE: To report the results of secondary posterior chamber intraocular lens (PC-IOL) implantation in pediatric cataract eyes with microcornea and/or microphthalmos.[ncbi.nlm.nih.gov] This disorder associated with axial myopia is an extremely rare ophthalmologic condition.[ncbi.nlm.nih.gov]

  • Cornelia De Lange Syndrome

    Congenital heart disease (CHD) is not a major criterion of the disease, but it affects many individuals.[ncbi.nlm.nih.gov] […] disabilities) 759.89 Marchesani (-Weill) syndrome (brachymorphism and ectopia lentis) 759.89 Meyer-Schwickerath and Weyers syndrome (dysplasia oculodentodigitalis) 759.89 Microphthalmos[icd9data.com] We performed entropion correction surgery, administered medical therapy for superficial keratitis and prescribed glasses for her myopia.[ncbi.nlm.nih.gov]

  • Lens Coloboma

    heart disease, and choanal atresia, growth or development retardation with multiple anomalies).[columbiaeye.org] Signs : typically in the 6 o'clock position, often associated with other defects, eg microphthalmos, due to failed closure of optic fissure.Atypically in another position[vetstream.com] Trupti Shreyans Gadiya, Gunjan Ingle Purpose : To describe case of aniridia with ptosis, lens coloboma, myopia & foveal hypoplasia.[urbanedge.co.in]

  • Coloboma

    heart disease polydactyly holoprosencephaly renal-coloboma syndrome Variants morning glory syndrome : optic nerve head coloboma with associated midline structural abnormalities[radiopaedia.org] Microcornea with microphthalmos had a worse prognosis than microcornea without microphthalmos (VA 3/60: 66.7% vs. 23.3%; unable to read N10: 66.7% vs. 34.1 %; no navigational[ncbi.nlm.nih.gov] He had recently noticed difficulty with distance vision and was found to have mild symmetric myopia. Best-corrected visual acuity was 20/20 in each eye.[link.springer.com]

  • Peters Anomaly

    There was developmental delay in 15 patients, congenital heart disease in eight patients, external ear abnormalities in five patients, structural defects of the central nervous[ncbi.nlm.nih.gov] […] reports are described to illustrate the unusual occurrence of dominant inheritance of Peters' anomaly and the concomitant occurrence of Peters' anomaly with colobomatous microphthalmos[jhu.pure.elsevier.com] Combined ocular anomalies were: microphthalmos (9x), myopia (4x), aniridia (2x), cataract (2x).[ncbi.nlm.nih.gov]

  • Syndromic Microphthalmia Type 10

    Heart Diseases (CHD) ZNF469 Zinc Finger Protein 469 Congenital Heart Diseases (CHD) Brittle Cornea Syndrome[bcm.edu] Diagnosis Code Q11.2 ICD-10: Q11.2 Short Description: Microphthalmos Long Description: Microphthalmos This is the 2019 version of the ICD-10-CM diagnosis code Q11.2 Valid[icdlist.com] AD - 154600 MARFAN SYNDROME Ectopia lentis, myopia AD FBN1 #154700 MASS SYNDROME (OVERLAP CONNECTIVE TISSUE DISEASE) Myopia - FBN1 #604308 MECKEL SYNDROME Iris colobma, hypertelorism[eyewiki.aao.org]

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