A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report

Sadeghmousavi, S; Shahkarami, S; Rayzan, E; Ahmed, S; Gharalari, FH; Rohlfs, M; Klein, C; Rezaei, N

Rezaei, N (通讯作者),Univ Tehran Med Sci, Immunol, Children Med Ctr Hosp, 62 Qarib St,Keshavarz Blvd, Tehran 14194, Iran.

ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS, 2022; 22 (8): 881

Abstract

Background: Chromosome Xp21 deletion syndrome is a rare X-linked recessive defect that occurs as a result of multiple gene deletions, including Glycer......

Full Text Link