MYOC

Glaucoma, Open Angle, Primary

Clinical Characteristics
Ocular Features: 

It has long been known from both clinical and genetic criteria that the disease called glaucoma is a heterogeneous condition. The common denominator is considered to be an optic neuropathy for which the primary risk factor is an elevation of intraocular pressure. However, the well-known clinical profile of glaucomatous retinal and optic nerve damage can also be found among patients without increased IOP and for these the cause remains elusive.  Ultimately, damage to retinal neurons and their axons result in loss of visual field and optic nerve volume with eventual blindness if untreated.

Systemic Features: 

No systemic abnormalities are consistently associated with primary open angle glaucoma.  However, glaucoma occurs in a large number of ocular and systemic disorders as well as chromosomal aberrations and in many such conditions there are anatomic abnormalities in the anterior chamber angle.  A variety of mainly anecdotal risk factors such as obesity, smoking, diabetes, migraines, stress and cardiovascular disease have been reported but their causative relationships have not been established.

Genetics

Primary open angle glaucoma likely consists of a collection of disorders resulting from an optic neuropathy.  Based on family data and ethnic distribution there can be little doubt that genes influence susceptibility to this disease.  In fact, 13 types have been described based on the unique chromosomal locations of mutations that have been associated with each.   Mutations in MYOC (1q23-q24) are responsible for a substantial proportion of POAG cases known as GLC1A through as yet unknown mechanisms.  Others types labeled GLC1B through GLC1O may result from specific mutations located on 10 different chromosomes.  In the absence of pedigrees with typical Mendelian inheritance patterns, it is reasonable to consider that the genes reported to be associated with POAG so far simply confer susceptibility to the optic neuropathy characteristic of clinical glaucoma (for further discussion see 137760).  Unidentified environmental factors in combination with other genes in individual genomes likely determine the degree of susceptibility in each person. 

Treatment
Treatment Options: 

Lowering of intraocular pressure remains the only clinical treatment available to lower the risk of POAG.  Unfortunately, this is not always effective, especially when the intraocular pressure is not significantly elevated.  There are no infallible guidelines for optimum pressure control and the therapy regimen must be tailored by follow-up monitoring of visual field and optic cup changes.  Once established, it is a lifelong disorder that requires active management.

Early detection is important in the management of glaucoma.  It is largely a 'silent' disease and the eye care professional cannot assume that absence of symptoms correlates with absence of disease.  A family history of glaucoma, especially in first degree relatives, as well as African American, Native American, and Hispanic ethnicity, and increased age are associated with an elevated risk of open angle glaucoma.  Patients belonging to such high risk groups should be monitored with regular examinations.

References
Article Title: 

Variants in the PRPF8 Gene are Associated with Glaucoma

Micheal S, Hogewind BF, Khan MI, Siddiqui SN, Zafar SN, Akhtar F, Qamar R, Hoyng CB, den Hollander AI. Variants in the PRPF8 Gene are Associated with Glaucoma. Mol Neurobiol. 2017 Jul 13. doi: 10.1007/s12035-017-0673-5. [Epub ahead of print].

PubMed ID: 
28707069

Open-angle glaucoma

Quigley HA. Open-angle glaucoma. N Engl J Med. 1993 Apr 15;328(15):1097-106. Review.

PubMed ID: 
8455668

Glaucoma, Open Angle, Juvenile

Clinical Characteristics
Ocular Features: 

Primary open angle glaucoma is a genetically and clinically heterogeneous condition.  The type described here often has its onset in juveniles, much earlier than the usual type, and is much more rare.  Onset is often in the second or third decade with an average age of onset of 18 years.  It is rare for this form of POAG to be diagnosed after 40 years of age.  IOP is commonly as high as 50 mmHg and the pressure is difficult to control.  Glaucomatous changes in the optic nerve progress rapidly. The usual pharmacologic agents can be helpful early but surgical control is often required.  Myopia is common (87%) but no anterior chamber anomalies are present.  Juvenile POAG is more common in African Americans.

Systemic Features: 

No systemic abnormalities have been reported.

Genetics

Juvenile onset open angle glaucoma, GLAC1A, is inherited in an autosomal dominant pattern with high penetrance.  It is caused by a mutation in MYOC located at 1q21-q31.  The usual adult onset glaucoma is caused by different mutations.

Pedigree: 
Autosomal dominant
Treatment
Treatment Options: 

The usual pharmacologic treatment may be effective in some, especially early, but some form of glaucoma filtration surgery is eventually required in over 80% of patients.

References
Article Title: 
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