CASE REPORT: CAYLER CARDIO-FACIAL SYNDROME: AN UNCOMMON CONDITION IN NEWBORNS

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.

PAWAR SUNIL JAYARAM; SHARMA DEEPAK KUMAR; SRILAKSHMI SELA; CHEJETI SUGUNA REDDY; PANDITA AAKASH

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

Journal Paper

Paper Information

Journal: Iranian Journal of Pediatrics Year:2015 | Volume:25 | Issue:2 Page(s): 1-3

Download Full-Text

View:

350

Download:

171

Cites:

Information Journal Paper

Title

CASE REPORT: CAYLER CARDIO-FACIAL SYNDROME: AN UNCOMMON CONDITION IN NEWBORNS

Author(s)

Keywords

CAYLER CARDIOFACIAL SYNDROME

CONGENITAL HEART DEFECT

Abstract

Introduction: Cayler cardio-facial syndrome is a rare syndrome associated with asymmetric crying faces with congenital heart disease. We report a newborn that was diagnosed as case of Cayler Cardio-facial syndrome based on clinical features and was confirmed with FISH analysis.Case Presentation: A term male baby, born to non-consanguineous couple through normal vaginal delivery was diagnosed to have asymmetric crying faces with deviation of angle of mouth to left side at the time of birth. The baby had normal faces while sleeping or silent. Mother was known case of hypothyroidism and was on treatment. Baby was diagnosed as case of Cayler Cardio-facial Syndrome and was investigated with echocardiogram, brain ultrasound, total body X-ray examination, X-ray of cervico-thoracic vertebral column and fundus examination. Echocardiogram showed muscular VSD, brain ultrasound was normal and fundus examination showed tortuous retinal vessels. Whole body X-ray and lateral X-ray of cervico-thoracic vertebral column were not suggestive of any skeletal abnormalities. The other associated malformation was right ear microtia. Baby FISH karyotype analysis showed deletion of 22q11.2 deletion. Baby was discharged and now on follow-up.Conclusions: Cayler syndrome is a rare syndrome which must be suspected if a baby has asymmetrical cry pattern and normal facies when baby sleeps. Patient must be evaluated with echocardiography to find out associated cardiac malformations. These infants should undergo FISH analysis for 22q11.2 deletion syndrome.

Cites

No record.

References

No record.

Cite

APA: Copy

PAWAR, SUNIL JAYARAM, SHARMA, DEEPAK KUMAR, SRILAKSHMI, SELA, CHEJETI, SUGUNA REDDY, & PANDITA, AAKASH. (2015). CASE REPORT: CAYLER CARDIO-FACIAL SYNDROME: AN UNCOMMON CONDITION IN NEWBORNS. IRANIAN JOURNAL OF PEDIATRICS, 25(2), 1-3. SID. https://sid.ir/paper/672017/en

Vancouver: Copy

PAWAR SUNIL JAYARAM, SHARMA DEEPAK KUMAR, SRILAKSHMI SELA, CHEJETI SUGUNA REDDY, PANDITA AAKASH. CASE REPORT: CAYLER CARDIO-FACIAL SYNDROME: AN UNCOMMON CONDITION IN NEWBORNS. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2015;25(2):1-3. Available from: https://sid.ir/paper/672017/en

IEEE: Copy

SUNIL JAYARAM PAWAR, DEEPAK KUMAR SHARMA, SELA SRILAKSHMI, SUGUNA REDDY CHEJETI, and AAKASH PANDITA, “CASE REPORT: CAYLER CARDIO-FACIAL SYNDROME: AN UNCOMMON CONDITION IN NEWBORNS,” IRANIAN JOURNAL OF PEDIATRICS, vol. 25, no. 2, pp. 1–3, 2015, [Online]. Available: https://sid.ir/paper/672017/en

Related Journal Papers

No record.

Related Seminar Papers

No record.

Related Plans

No record.

Recommended Workshops