EXTENSIVE MONGOLIAN SPOTS WITH AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT

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.

YC BEEREGOWDA; BV NAVEEN KUMAR; YC MANJUNATHA

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

Journal Paper

Paper Information

Journal: Iranian Journal of Pediatrics Year:2012 | Volume:22 | Issue:2 Page(s): 252-254

Download Full-Text

View:

305

Download:

183

Cites:

Information Journal Paper

Title

EXTENSIVE MONGOLIAN SPOTS WITH AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT

Author(s)

YC BEEREGOWDA | BV NAVEEN KUMAR | YC MANJUNATHA | Issue Writer Certificate

Keywords

MONGOLIAN SPOTS

DERMAL MELANOCYTOSIS

INBORN ERROR OF METABOLISM

BIRTH MARKS

Abstract

Background: MONGOLIAN SPOTS are benign skin markings at birth which fade and disappear as the child grows. Often persistent extensive MONGOLIAN SPOTS are associated with INBORN ERROR OF METABOLISM. We report thirteen people of the single family manifested with extensive MONGOLIAN SPOTS showing autosomal dominant inheritance.Case Presentation: A one day old female child, product of second degree consanguineous marriage, born by normal vaginal delivery with history of meconium stained amniotic fluid and birth asphyxia. On examination the child showed extensive bluish discoloration of the body involving trunk and extremities in both anterior and posterior aspects associated with bluish discoloration of the tongue. A detailed family history revealed most of the family members manifested with extensive bluish discoloration of the body soon after birth which faded in the first few years of life and completely disappeared by puberty. Thus it was diagnosed to be extensive MONGOLIAN SPOTS with an autosomal dominant inheritance.Conclusion: Knowledge about the natural history of extensive MONGOLIAN SPOTS, their inheritance and association with certain metabolic diseases mainly IEM and Mucopolysaccharidosis aids in the diagnosis and in order to improve the patient’s prognosis.

Cites

No record.

References

No record.

Cite

APA: Copy

YC, BEEREGOWDA, BV, NAVEEN KUMAR, & YC, MANJUNATHA. (2012). EXTENSIVE MONGOLIAN SPOTS WITH AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS, 22(2), 252-254. SID. https://sid.ir/paper/572227/en

Vancouver: Copy

YC BEEREGOWDA, BV NAVEEN KUMAR, YC MANJUNATHA. EXTENSIVE MONGOLIAN SPOTS WITH AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2012;22(2):252-254. Available from: https://sid.ir/paper/572227/en

IEEE: Copy

BEEREGOWDA YC, NAVEEN KUMAR BV, and MANJUNATHA YC, “EXTENSIVE MONGOLIAN SPOTS WITH AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT,” IRANIAN JOURNAL OF PEDIATRICS, vol. 22, no. 2, pp. 252–254, 2012, [Online]. Available: https://sid.ir/paper/572227/en

Related Journal Papers

No record.

Related Seminar Papers

No record.

Related Plans

No record.

Recommended Workshops