MYOTONIA CHONDRODYSTROPHIA FIRST CASE OF LOGHMAN HAKIM HOSPITAL

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

BEHVAD A.; LESANI M.; GOLKARI H.; FALAH AZAR

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Research in Medicine Year:2001 | Volume:25 | Issue:3 Page(s): 195-198

Download Full-Text

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

View:

825

Download:

Cites:

Information Journal Paper

Title

MYOTONIA CHONDRODYSTROPHIA FIRST CASE OF LOGHMAN HAKIM HOSPITAL

Author(s)

BEHVAD A. | LESANI M. | GOLKARI H. | FALAH AZAR | Issue Writer Certificate

Keywords

MYOTONIA CHONDRODYSTROPHIAQ4

CHILDRENQ4

Abstract

MYOTONIA CHONDRODYSTROPHIA, which is easier to diagnose than describe, is a rare congenital disorder inherited as an autosomal recessive. Myotonia is accompanied by chondrodystrophia and epiphyseal dysplasia. Affected individuals are presenting with growth retardation, pectus carinatum, sadly appearance of face, blepharophimosis, ear and dental abnormalities, puckered lips, and hypertrophic muscles. Articular contractures especially in elbow are existing and patients had problems in gait. EMG changes are usually used to differentiate it from congenital myotonia. Immune deficiency disorders are not noted and its etiology is still remained unknown. Therapeutic affaires are of less importance. Case report: we have presented an 8-year old boy referring due to facial deformity. His parents have stated that he had facial deformity and problems in gait since 6 years ago. His problem had progressive course. He had problems in sitting, standing up, and going up stairs, but he had never fallen down. His past medical history has revealed nothing. Now, he is studying in primary school and is a good student, too. His parents were not relevant. He is the second child and the other two CHILDREN are normal. He has the following indices: Body weight: 21kg, height: 116cm, head circumference: 52 cm, chest: 80cm, BP: 100/60 mmHg, T:37.1°c.

Cites

No record.

References

No record.

Cite

APA: Copy

BEHVAD, A., LESANI, M., GOLKARI, H., & FALAH, AZAR. (2001). MYOTONIA CHONDRODYSTROPHIA FIRST CASE OF LOGHMAN HAKIM HOSPITAL. PAJOUHESH DAR PEZESHKI, 25(3), 195-198. SID. https://sid.ir/paper/41817/en

Vancouver: Copy

BEHVAD A., LESANI M., GOLKARI H., FALAH AZAR. MYOTONIA CHONDRODYSTROPHIA FIRST CASE OF LOGHMAN HAKIM HOSPITAL. PAJOUHESH DAR PEZESHKI[Internet]. 2001;25(3):195-198. Available from: https://sid.ir/paper/41817/en

IEEE: Copy

A. BEHVAD, M. LESANI, H. GOLKARI, and AZAR FALAH, “MYOTONIA CHONDRODYSTROPHIA FIRST CASE OF LOGHMAN HAKIM HOSPITAL,” PAJOUHESH DAR PEZESHKI, vol. 25, no. 3, pp. 195–198, 2001, [Online]. Available: https://sid.ir/paper/41817/en

Related Journal Papers