Smith-magenis syndrome: A rare case report

Autor: Rupam Sinha, Harshvardhan Jha, Debarati Deb, Mainak Datta

Publikováno v: Journal of Family Medicine and Primary Care, Vol 11, Iss 3, Pp 1191-1194 (2022)

Smith-Magenis syndrome is a rare genetic disorder involving multiple body systems, along with mental retardation and sleep disturbances. It is attributed to micro deletion at 17p11.2 chromosome region encoding for RAI1 gene. This article presents a c

Externí odkaz: https://doaj.org/article/1a1a3f4c3a274feeb5a8b80c858c3889

Smith-magenis syndrome: A rare case report.

Autor: Sinha R; Department of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India., Jha H; Department of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India., Deb D; Department of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India., Datta M; Department of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India.

Publikováno v: Journal of family medicine and primary care [J Family Med Prim Care] 2022 Mar; Vol. 11 (3), pp. 1191-1194. Date of Electronic Publication: 2022 Mar 10.