Create issue ticket

10 Possible Causes for Cataracts Usually Congenital, Congenital Eye Anomaly, Globulins Increased

  • Congenital Rubella Syndrome

    Congenital rubella syndrome is characterized by the triad of deafness, cataract and cardiovascular malformations.[] […] exposed to measles; increasing the recommended dose of IGIM for immunocompetent persons; and recommending use of immune globulin administered intravenously (IGIV) for severely[] .  Rate of organ anomalies in CRS 5.  The classic triad for congenital rubella syndrome is:  Sensorineural deafness (58% of patients)  Eye abnormalities especially pigmentary[]

  • Hallermann-Streiff Syndrome

    […] bilateral congenital cataracts, and microphthalmia.[] Low urinary 17-hydroxy and 17ketosteroid excretion and increased serum gamma globulin are mentioned in a few instances.5 It is of interest that pituitary function, when studied[] Hallermann-Streiff syndrome is a rare congenital disorder characterized as a complex association of developmental anomalies involving structures of ectodermal origin (the[]

  • Oculocerebrorenal Syndrome

    The hallmark of this disorder is the appearance of congenital bilateral cataracts (thick clouding of the lenses) that are usually deemed visually significant at birth.[] […] serum concentrations of the α 2 -globulin fraction on serum electrophoresis.[] The classical diagnostic triad includes: Congenital cataracts Neonatal or infantile hypotonia with subsequent mental impairment Renal tubular dysfunction progressing to chronic[]

  • Familial Congenital Nasolacrimal Duct Obstruction

    (cone-shaped cornea) Congenital cataracts Blepharitis Conjunctivitis Lacrimal duct obstruction Retinal abnormalities The following may be helpful for families: Hearing and[] The common denominator is a decrease in androgens, from either reduced ovarian function (in postmenopausal women) or increased levels of the sex hormone–binding globulin ([] WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5 Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies (type A), which includes both the more severe[]

  • Congenital Neutropenia

    In this form, with dominant transmission related to the mutation in the dynamin 2 gene, neurological signs are sometimes discreet and are accompanied by congenital cataract[] The gamma globulin protein level in blood is low. The inheritance of the disease is autosomal recessive.[] New Tests Hydrocephalus, Congenital 2 with or without Brain or Eye Anomalies via MPDZ Gene Sequencing with CNV Detection ( #12013 ) Pediatric Cancer Sequencing Panel with[]

  • Retinoblastoma

    Other eye diseases which can cause these symptoms include congenital cataract, Toxocara canis, Coat’s disease, and persistent hypertrophic primary vitreous (PHPV).[] The vitreous may have multiple areas of 'floating' debris, which may represent vitreous seeding or, alternatively, necrotic debris, hemorrhage or increased globulin content[] Persistent hyperplastic primary vitreous is a congenital developmental anomaly of the eye resulting from failure of the embryological, primary vitreous, and hyaloid vasculature[]

  • Spastic Ataxia with Congenital Miosis

    It is usually recognisable at birth and typically presents with congenital cataracts, often with bilateral microphthalmia.[] Cerebrospinal fluid findings include a slight mononuclear pleocytosis, increased globulin content, and positive Wasserman reaction.[] […] muscular alpha-dystroglycanopathy with brain and eye anomalies Congenital neuronal ceroid lipofuscinosis Congenital toxoplasmosis Constitutional megaloblastic anemia with[]

  • Muscular Dystrophy-Dystroglycanopathy Type A2

    Walker-Warburg Syndrome Clinical Characteristics Ocular Features: The eyes are usually small and contain either retinal dysplasia or a congenital retinal detachment.[] Diagnosis MH presents with tachycardia, muscle rigidity (caused by muscle contracture that may progress to rigor or death), increased muscle permeability (resulting in increased[] Name muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1 FlyBase ID FBhh0000278 Disease Ontology Term Parent Disease In humans, multiple[]

  • Cataract - Ataxia - Short Stature - Mental Retardation (CASM)

    Dislocated lens (usually superiorly and nasally) Severe refractive errors Megalocornea (front third of the eye is larger than normal) Cataracts Uveal colobomas Secondary glaucoma[] . • Diagnosis – demonstration of an increased antibody titre, usually associated with increased g –globulin concentrations, in the CSF. • Intraventricular interferon-alfa[] Mutation in the GMPPB gene can also cause a more severe congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies (type A14; MDDGA14; 615350) and a less[]

  • Thyro-Cerebro-Renal Syndrome

    Dislocated lens (usually superiorly and nasally) Severe refractive errors Megalocornea (front third of the eye is larger than normal) Cataracts Uveal colobomas Secondary glaucoma[] Total cholesterol and triglyceride levels are typically increased.[] Reduced clearance rate of thyroxine-binding globulin (TBG) with increased sialylation: a mechanism for estrogen-induced elevation of serum TBG concentration . J. Clin.[]

Similar symptoms