TWO SISTERS WITH CONGENITAL MYASTHENIA SYNDROME: CASE REPORT

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SOLTAN SANJARI M.; BAHMANI KASHKOULI M.; PARVARESH M.M.

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Journal: BINA Year:2005 | Volume:10 | Issue:5 (41) Page(s): 637-640

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Information Journal Paper

Title

TWO SISTERS WITH CONGENITAL MYASTHENIA SYNDROME: CASE REPORT

Author(s)

SOLTAN SANJARI M. | BAHMANI KASHKOULI M. | PARVARESH M.M. | Issue Writer Certificate

Keywords

CONGENITAL MYASTHENIA SYNDROMEQ3

CASE REPORTQ3

Abstract

Purpose: To report two sisters with CONGENITAL MYASTHENIA SYNDROME (CMS) masquerading as myasthenia gravis.Patients and findings: Two six and seven years old sisters presented with variable strabismus, ptosis, and fatigue. All symptoms were aggravated with exercise and improved with rest. Intramuscular prostigmin injection decreased their symptoms. A diagnosis of CMS was made according to early onset (infancy), familial pattern, and lack of serum antibodies. Oral neostigmin was begun for treatment. Conclusion: Although CMS is a rare disorders, they should be considered in all cases with variable strabismus and ptosis.

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APA: Copy

SOLTAN SANJARI, M., BAHMANI KASHKOULI, M., & PARVARESH, M.M.. (2005). TWO SISTERS WITH CONGENITAL MYASTHENIA SYNDROME: CASE REPORT. BINA, 10(5 (41)), 637-640. SID. https://sid.ir/paper/42980/en

Vancouver: Copy

SOLTAN SANJARI M., BAHMANI KASHKOULI M., PARVARESH M.M.. TWO SISTERS WITH CONGENITAL MYASTHENIA SYNDROME: CASE REPORT. BINA[Internet]. 2005;10(5 (41)):637-640. Available from: https://sid.ir/paper/42980/en

IEEE: Copy

M. SOLTAN SANJARI, M. BAHMANI KASHKOULI, and M.M. PARVARESH, “TWO SISTERS WITH CONGENITAL MYASTHENIA SYNDROME: CASE REPORT,” BINA, vol. 10, no. 5 (41), pp. 637–640, 2005, [Online]. Available: https://sid.ir/paper/42980/en

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