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Paper Information

Journal:   IRANIAN JOURNAL OF PEDIATRICS   Spring 2003 , Volume 13 , Number 1; Page(s) 37 To 41.
 
Paper: 

CYSTINOSIS: REPORT OF A CASE

 
 
Author(s):  IMANZADEH F., SALEHPOUR SH., NARIMAN SH., SAYYARI A.A.
 
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Abstract: 

Cystinosis is a hereditary autosomal recessive metabolic disorder in which increased cellular absorption of cystine causes its accumulation in lysozymes. Cystine is accumulated in reticuloendothelial cells of kidneys, cornea, and sclera as well as fibroblasts and leukocytes. This leads to development of the typical clinical symptoms.
The incidence rate of the disease is 1/26000 to 1/200000.
We report on an 8-month-old boy presenting with poor weight gain, anorexia, polydypsia, polyuria, restlessness, calmness in low-light environment, frequent vomiting and disturbance in bowel movements.
A sibling of the child and an uncle of his expired of the same disease.
Cystine crystals were observed in bone marrow smears and in corneae cystine precipitations were seen with slit lamp.
It is recommended to think to metabolic disorders, especially cystinosis, in children presenting with polydipsia and polyuria.

 
Keyword(s): CYSTINOSIS, METABOLIC DISEASE, HEREDITARY DISEASE, POLYDYPSY, POLYURIA
 
 
References: 
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Citations: 
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+ Click to Cite.
APA: Copy

IMANZADEH, F., & SALEHPOUR, S., & NARIMAN, S., & SAYYARI, A. (2003). CYSTINOSIS: REPORT OF A CASE. IRANIAN JOURNAL OF PEDIATRICS, 13(1), 37-41. https://www.sid.ir/en/journal/ViewPaper.aspx?id=14177



Vancouver: Copy

IMANZADEH F., SALEHPOUR SH., NARIMAN SH., SAYYARI A.A.. CYSTINOSIS: REPORT OF A CASE. IRANIAN JOURNAL OF PEDIATRICS. 2003 [cited 2021June20];13(1):37-41. Available from: https://www.sid.ir/en/journal/ViewPaper.aspx?id=14177



IEEE: Copy

IMANZADEH, F., SALEHPOUR, S., NARIMAN, S., SAYYARI, A., 2003. CYSTINOSIS: REPORT OF A CASE. IRANIAN JOURNAL OF PEDIATRICS, [online] 13(1), pp.37-41. Available: https://www.sid.ir/en/journal/ViewPaper.aspx?id=14177.



 
 
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