Glaucoma as an early complication of Hurler's disease.
Explore this paper's citation graph
Summary
Three cases of Hurler's disease in which glaucoma developed in early childhood are reported in which the condition may be a commonly unrecognised early complication of this condition.
- Type
- article
- Published
- 1988-09-01
- Cited by
- 39
- References
- 8
- Access
- Open access
- OpenAlex
- https://openalex.org/W2012188139
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:21074082
Keywords
Medicine, Glaucoma, Complication, Hurler syndrome, Disease
References
- Hyaluronidase effects on aqueous outflow resistance. Quantitative and localizing studies in the rhesus monkey eye.
- Mechanism of the aqueous outflow across the trabecular wall of Schlemm's canal.
- Glaucoma in a case of Hurler disease.
- Ring chromosome 18 in mother and daughter.
- Acute glaucoma in systemic mucopolysaccharidosis I-S.
- Application of electron microscopy to the study of ocular inborn errors of metabolism.
- [Mucopolysaccharidoses].
Cited by
- Handbook of pediatric eye and systemic disease
- The Autophagic Lysosomal System in Outflow Pathway Physiology and Pathophysiology
- Ocular manifestations and management recommendations of lysosomal storage disorders I: mucopolysaccharidoses
- Ocular manifestations in the mucopolysaccharidoses – a review
- Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management
- Comparison of Rebound Tonometry, Perkins Applanation Tonometry and Ocular Response Analyser in Mucopolysaccharidosis Patients
- The ocular features of the mucopolysaccharidoses
- Assessment and diagnosis of suspected glaucoma in patients with mucopolysaccharidosis
- Intraocular pressure change in orbital disease.
- Corneal hysteresis in mucopolysaccharidosis I and VI
- Normal intraocular pressure after a bone marrow transplant in glaucoma associated with mucopolysaccharidosis type I-H.
- THE ROLE OF PROTEOLYTIC CELLULAR SYSTEMS IN TRABECULAR MESHWORK HOMEOSTASIS
- Grouped papules in Hurler-Scheie syndrome.
- Clinical classification of childhood glaucomas.
- Mucopolysaccharidoses and the eye.
- Clinical guidelines for diagnosing and managing ocular manifestations in children with mucopolysaccharidosis
- Ocular manifestations as key features for diagnosing mucopolysaccharidoses.
- Diagnosis and management of ophthalmological features in patients with mucopolysaccharidosis
- Involvement of the Anterior Segment of the Eye in Patients with Mucopolysaccharidoses: A Review of Reported Cases and Updates on the Latest Diagnostic Instrumentation
- Influence of Corneal Opacity on Intraocular Pressure Assessment in Patients with Lysosomal Storage Diseases
Related papers
- The Beginning of the End of Allogeneic Transplantation for Hurler Syndrome?
- Automated perimetry, tonometry, and questionnaire in glaucoma screening.
- Metachromatic cells in the gingiva in Hurler's syndrome.
- Glaucoma and Glaucoma Medications
- HURLER SYNDROME: 15 YEARS OF HEMATOPOIETIC STEM CELL TRANSPLANTATION WITH HURLER SYNDROME AT THE RUSSIAN CHILDREN’S CLINICAL HOSPITAL
- Increased Longevity and Metabolic Correction Following Syngeneic Bone Marrow Transplantation in a Murine Model of Mucopolysaccharidosis Type I
- Laronidase Treatment of Mucopolysaccharidosis I
- Two familial cases of high blood galactose of unknown aetiology
- Hematopoietic cell transplantation in Hurler syndrome. Optimizing the safety and efficacy
- 3-LbNets: Tri-Labeling Deep Convolutional Neural Network for the Automated Screening of Glaucoma, Glaucoma Suspect, and No Glaucoma in Fundus Images