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    Topic review

    Stormorken syndrome

    Subjects: Genetics
    View times: 5
    Submitted by: Bruce Ren
    (This entry belongs to Entry Collection "MedlinePlus ")

    Definition

    Stormorken syndrome is a rare condition that affects many body systems.

    1. Introduction

    Stormorken syndrome is a rare condition that affects many body systems. Affected individuals usually have thrombocytopenia, in which there are abnormally low numbers of blood cells called platelets. Platelets are involved in normal blood clotting; a shortage of platelets typically results in easy bruising and abnormal bleeding. In addition, affected individuals often have a muscle disorder, called tubular aggregate myopathy, that leads to muscle weakness. Another feature of Stormorken syndrome is permanent constriction of the pupils of the eyes (miosis), which may be caused by abnormalities in the muscles that control the size of the pupils. Other features include lack of a functioning spleen (asplenia), scaly skin (ichthyosis), headaches, and difficulty with reading and spelling (dyslexia).

    2. Frequency

    Stormorken syndrome is a rare disorder. Approximately a dozen cases have been reported in the medical literature.

    3. Causes

    Stormorken syndrome is caused by a mutation in the STIM1 gene. The protein produced from this gene is involved in controlling the entry of positively charged calcium atoms (calcium ions) into cells. The STIM1 protein recognizes when calcium ion levels are low and stimulates the flow of ions into the cell through special channels in the cell membrane called calcium-release activated calcium (CRAC) channels. The flow of calcium ions through CRAC channels triggers signaling within cells that helps control gene activity, cell growth and division, and immune function.

    The STIM1 gene mutation involved in Stormorken syndrome leads to production of a STIM1 protein that is constantly turned on (constitutively active), which means it continually stimulates calcium ion entry through CRAC channels regardless of ion levels. Researchers suggest that the abnormal ion flow in platelets causes them to break down earlier than usual, leading to thrombocytopenia and bleeding problems in people with Stormorken syndrome. It is unknown how constitutively active STIM1 leads to the other features of the disorder.

    4. Inheritance

    This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In some cases, an affected person inherits the mutation from one affected parent. Other cases result from new mutations in the gene and occur in people with no history of the disorder in their family.

    5. Other Names for This Condition

    • Stormorken-Sjaastad-Langslet syndrome
    • thrombocytopathy, asplenia, and miosis

    The entry is from https://medlineplus.gov/genetics/condition/stormorken-syndrome

    References

    1. Kilch T, Alansary D, Peglow M, Dörr K, Rychkov G, Rieger H, Peinelt C,Niemeyer BA. Mutations of the Ca2+-sensing stromal interaction molecule STIM1regulate Ca2+ influx by altered oligomerization of STIM1 and by destabilizationof the Ca2+ channel Orai1. J Biol Chem. 2013 Jan 18;288(3):1653-64. doi:10.1074/jbc.M112.417246.
    2. Misceo D, Holmgren A, Louch WE, Holme PA, Mizobuchi M, Morales RJ, De PaulaAM, Stray-Pedersen A, Lyle R, Dalhus B, Christensen G, Stormorken H, TjønnfjordGE, Frengen E. A dominant STIM1 mutation causes Stormorken syndrome. Hum Mutat.2014 May;35(5):556-64. doi: 10.1002/humu.22544.
    3. Morin G, Bruechle NO, Singh AR, Knopp C, Jedraszak G, Elbracht M,Brémond-Gignac D, Hartmann K, Sevestre H, Deutz P, Hérent D, Nürnberg P, Roméo B,Konrad K, Mathieu-Dramard M, Oldenburg J, Bourges-Petit E, Shen Y, Zerres K,Ouadid-Ahidouch H, Rochette J. Gain-of-Function Mutation in STIM1 (P.R304W) IsAssociated with Stormorken Syndrome. Hum Mutat. 2014 Oct;35(10):1221-32. doi:10.1002/humu.22621.
    4. Nesin V, Wiley G, Kousi M, Ong EC, Lehmann T, Nicholl DJ, Suri M, Shahrizaila N, Katsanis N, Gaffney PM, Wierenga KJ, Tsiokas L. Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis. Proc Natl Acad Sci U S A. 2014 Mar 18;111(11):4197-202. doi:10.1073/pnas.1312520111.
    5. Parekh AB. Local Ca2+ influx through CRAC channels activates temporally andspatially distinct cellular responses. Acta Physiol (Oxf). 2009 Jan;195(1):29-35.doi: 10.1111/j.1748-1716.2008.01919.x.
    6. Stormorken H, Sjaastad O, Langslet A, Sulg I, Egge K, Diderichsen J. A newsyndrome: thrombocytopathia, muscle fatigue, asplenia, miosis, migraine, dyslexiaand ichthyosis. Clin Genet. 1985 Nov;28(5):367-74.
    7. Zhou Y, Meraner P, Kwon HT, Machnes D, Oh-hora M, Zimmer J, Huang Y, Stura A, Rao A, Hogan PG. STIM1 gates the store-operated calcium channel ORAI1 in vitro.Nat Struct Mol Biol. 2010 Jan;17(1):112-6. doi: 10.1038/nsmb.1724.
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