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404 Possible Causes for Joint Stiffness, Microphthalmos, Myopia

  • 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] CMD results in overall muscle weakness with possible joint stiffness or looseness.[mda.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]

  • Pfeiffer-Palm-Teller Syndrome

    Aughton syndrome 0 *Abnormalities, Multiple *Cleft Palate *Dextrocardia *Intellectual Disability *Microphthalmos.[reference.md] Stiffness, and High-Pitched Voice Annotation Sufficiency: ?[monarchinitiative.org] Night blindness skeletal anomalies unusual facies 0 *Myopia *Night Blindness *Facies.[reference.md]

  • Retinal Degeneration-Nanophthalmos-Glaucoma Syndrome

    microphthalmos) or posterior segment (posterior microphthalmos; (PM) of eyeball.[nature.com] Related symptoms: Autosomal recessive inheritance Short stature Brachydactyly Myopia Joint stiffness SOURCES: MONDO UMLS OMIM More info about WEILL-MARCHESANI SYNDROME 3;[mendelian.co] Based on biometric data harmonious microphthalmos is differentiated of posterior microphthalmos.[egms.de]

  • Marchesani-Weill 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] English Weill-Marchesani syndrome autosomal genetic disease characterized by short stature, bachycephaly and other facial abnormalities, brachydactyly, joint stiffness and[wikidata.org] 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

    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] stiffness Retinal atrophy Abnormal aldolase level Clitoral hypoplasia Fine hair Corneal opacity Dysphonia Brittle hair Osteoporosis Decreased antibody level in blood Bilateral[mendelian.co] This disorder associated with axial myopia is an extremely rare ophthalmologic condition.[ncbi.nlm.nih.gov]

  • 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] It is associated with learning difficulties, diminished sex hormones, and stiffness of the muscles and joints.[verywell.com] Glaucoma • Stargardt’s Syndrome • Retinal Detachment • Optic Neuritis • Diabetic Retinopathy • Retinitis Pigmentosa • Optic Nerve Atrophy • Cataracts • Usher’s Syndrome • Myopia[pinterest.cl]

  • Isolated Congenital Sclerocornea

    The condition is often associated with other local and systemic anomalies like microphthalmos, anomalies a t the angle of the anterior chamber (Franceschetti, 1946; Goldstein[documents.tips] stiffness [ 25 ].[journals.plos.org] 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.org]

  • Syndromic Microphthalmia Type 10

    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] stiffness Arthrogryposis multiplex congenita Limb muscle weakness Talipes Distal amyotrophy Peripheral axonal neuropathy Limitation of joint mobility Paralysis Elbow flexion[mendelian.co] 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]

  • Malignant Hyperthermia - Arthrogryposis - Torticollis

    […] epilepsy Microcephaly mesobrachyphalangy tracheoesophageal fistula syndrome Microcephaly microcornea syndrome Seemanova type Microcephaly micropenis convulsions Microcephaly microphthalmos[en.wikipedia.org] stiffness Trismus Hyperhidrosis Generalized hirsutism Anxiety Splenomegaly Respiratory arrest High pitched voice Nasal speech Ventricular hypertrophy Limb muscle weakness[mendelian.co] Microcephaly microphthalmos blindness[?] Microcephaly nonsyndromal[?] Microcephaly pontocerebellar hypoplasia dyskinesia[?][encyclopedia.kids.net.au]

  • Stickler 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] Joint problems Hypermobility (looseness and overflexibility of joints). Stiffness and premature arthritis. Prominent joints - joints that are more visible than normal.[contact.org.uk] In the third family, all patients had a marfanoid habitus, high myopia, and mental retardation.[ncbi.nlm.nih.gov]

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