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Congenital Stationary Night Blindness

6 people found, showing 1 to 6

To save room on the page we use the term disabled to indicate those with disabilities, special need or a medical condition.

 

Australia ( Australasia )

Jan 1987  male
Family type: two parent family
Siblings: 0
Disabled siblings: 0
Username: Andy87
Relationship: Male - Same Person
Other conditions: None

Last updated: 08 Feb 2008
Brief summary: I have congenital stationary night blindness, and thought I could help answer any questions parents may have in regards to this condition.

Belgium ( Rest of Europe )

Oct 1983  male
Family type: two parent family
Siblings: 3
Disabled siblings: 1
Username: piquart
Relationship: Male - Same Person
Other conditions: None

Last updated: 15 Mar 2009
Brief summary: I've CSNB-2 (or incomplete CSNB X-linked) and now, I'm studiing this pathology as a Master in Biology for a PhD project

Canada ( Americas )

Mar 1975  male
Family type: two parent family
Siblings: 0
Disabled siblings: 0
Username: MicknMarty
Relationship: Mother
Other conditions: None

Last updated: 29 Aug 2007
Brief summary: My son has congenital stationary night blindness and we are hoping to contact others with this condition so we can help each other for everyones benefit.

location not given

Jun 2002  male
Family type: two parent family
Siblings: 1
Disabled siblings: 0
Username: Maryan
Relationship: Mother
Other conditions: None

Last updated: 19 Aug 2005
Brief summary: My second son has congenital stationary night blindness and severe developmental delay. He is a happy little boy now, despite a very troubled start to life!

Feb 2002  male
Family type: two parent family
Siblings: 1
Disabled siblings: 2
Username: spongbob
Relationship: Mother
Other conditions: None

Last updated: 12 Oct 2005
Brief summary: Both my boys have stationary night blindness, would like to chatt to other parents whos children have the same condition.

United States of America ( Americas )

Jul 2003  male
Family type: two parent family
Siblings: 1
Disabled siblings: 1
Username: nitesite
Relationship: Mother
Other conditions: None

Last updated: 01 May 2007
Brief summary: We have a son and daughter that have both been diagnosed with congenital stationary night blindness. They are approaching teenage years, and have done quite well so far. I would love to hear from other parents of kids with the same condition.

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Related conditions 

There are conditions similar or related to this one that have people listed against them. They are listed below. If there are UK Support groups available, they will be indicated by this G icon. Click this icon to view the list of available support groups.

Condition (also listed as) No. of members Support Group
3rd Nerve Palsy of the Eye 2 -
Achromatopsia 0 -
Acute Zonal Occult Outer Retinopathy (AZOOR) 0 -
Adie Syndrome (Holmes-Adie Syndrome) 2 -
Ametropia 0 -
Aniridia (Congenital Abnormality of the Iris) 13 -
Anophthalmia (Heminasal Aplasia) 4 G
Axenfeld Syndrome (Axenfeld Anomaly; Axenfeld-Rieger Syndrome; Rieger Syndrome) 0 -
Axenfeld-Schürenberg Syndrome (Cyclic Oculomotor Paralysis; Congenital Cyclic Oculomotor Paralysis) 0 -
Cataracts 20 G
Choroideremia 0 -
Chromotosia Congenita 0 -
Coats' Disease (Exudative Retinitis) 8 -
Coloboma 13 -
Colourblindness 0 -
Cone Dystrophy (Combined Cone-Rod Degeneration; Progressive Cone-Rod Degeneration; Cone-Rod Dystrophy; Retinal Cone Degeneration; Retinal Cone Dystrophy; Retinal Cone-Rod Dystrophy) 1 -
Corneal Dystrophy 5 -
Eales Disease 1 -
Familial exudative vitreoretinopathy (FEVR) 2 -
Glaucoma 10 G
Homonymous Hemianopia 6 -
Idiopathic Optic Atrophy 1 -
Keratoconus 2 G
Macular Disease 0 G
Macular Dystrophy 1 -
Microphthalmia 5 -
Nystagmus (Spasmus nutans,Congenital Idiopathic Nystagmus) 21 G
Nystagmus and Astigmatism 7 -
Ocular Disorders (Drusen Syndrome) 0 -
Optic Nerve Atrophy 6 -
Optic Nerve Dysplasia 2 -
Optic Nerve Hypoplasia 20 -
Persistant Hyperplastic Primary Vitreous 2 -
Peter's Anomaly 7 -
Peter's Plus Syndrome (Peter's Plus Anomaly) 11 -
Pigment Epithelium retinal detachment 0 -
Post Polymorhous Corneal Dystrophy 0 -
Reis-Büclers (Reis-Bncklers) 0 -
Retinitis Pigmentosa (Bulls Eye Dystrophy; Central Areola Choroidal Dystrophy; Retinal Dystrophy, Tapeto Retinal Degenaration) 2 G
Retinopathy of Prematurity 1 -
Rieger's Anomaly 1 -
Rod Monochromatisim 0 -
Sclerocornea 3 -
Spheromicrophakia 0 -
Thyroid Eye Disease (Thyroid Ophthalmopathy; Thyroid Associated Ophthalmopathy; Graves' Eye Disease; Graves' Ophthalmopathy ) 1 G
Uveitis 1 G

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