Glaucoma in the Maroteaux-Lamy syndrome.
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Summary
The findings suggest that glaucoma may be more common in the Maroteaux-Lamy syndrome than has been realized and that the initial mechanism is secondary acute or chronic angle closure not related to pupillary block.
- Type
- article
- Published
- 1989-10-01
- Cited by
- 45
- References
- 8
- OpenAlex
- https://openalex.org/W2010472479
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:39634809
Keywords
Glaucoma, Gonioscopy, Ophthalmology, Medicine, Iridectomy
References
- Acid mucopolysaccharides in the outflow apparatus.
- Ultrastructural and histochemical studies of a newly recognized form of systemic mucopolysaccharidosis. (Maroteaux-Lamy syndrome, mild phenotype).
- Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years. (Maroteaux‐Lamy syndrome, type B)
- Hydrocephalus and papilledema in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI).
- Glaucoma in a case of Hurler disease.
- Acute glaucoma in systemic mucopolysaccharidosis I-S.
- Ocular pathology of the Maroteaux-Lamy syndrome (systemic mucopolysaccharidosis type VI). Histologic and ultrastructural report of two cases.
Cited by
- Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma with Trisomy 8q22-Qter/ Monosomy 9p23-Pter
- Ocular manifestations in the mucopolysaccharidoses – a review
- Anatomy and physiology of the human eye: effects of mucopolysaccharidoses disease on structure and function – a review
- Comparison of Rebound Tonometry, Perkins Applanation Tonometry and Ocular Response Analyser in Mucopolysaccharidosis Patients
- Cultured porcine trabecular meshwork cells display altered lysosomal function when subjected to chronic oxidative stress.
- In Vivo Microstructural Analysis of the Cornea in Maroteaux-Lamy Syndrome
- The ocular features of the mucopolysaccharidoses
- Assessment and diagnosis of suspected glaucoma in patients with mucopolysaccharidosis
- Visual Dysfunction of Type I and VI Mucopolysaccharidosis Patients Evaluated with Visual Evoked Cortical Potential
- Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVA
- Central corneal thickness and its relationship to intraocular pressure in mucopolysaccararidoses-1 following bone marrow transplantation.
- Mucopolysaccharidosis VI (Maroteaux‐Lamy Syndrome) with Hearing Impairment and Pupillary Membrane Remnants
- EARLY OCULAR FINDINGS IN A PATIENT OF MAROTEAUX-LAMY SYNDROME
- Central Corneal Thickness in Mucopolysaccharidosis II and VI
- Does enzyme replacement therapy influence the ocular changes in type VI mucopolysaccharidosis?
- THE ROLE OF PROTEOLYTIC CELLULAR SYSTEMS IN TRABECULAR MESHWORK HOMEOSTASIS
- Ocular manifestation of storage diseases
- Mucopolysaccharidoses and the eye.
- Clinical guidelines for diagnosing and managing ocular manifestations in children with mucopolysaccharidosis
- Ocular manifestations as key features for diagnosing mucopolysaccharidoses.
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