The First Case Report of Kabuki Syndrome from the National Iranian Registry of Primary Immunodeficiencies

(E-pub Ahead of Print)

Author(s): Molood Safarirad, Ali Abbaszadeh Ganji, Saba Fekrvand, Reza Yazdani, Ahmad Vosughi Motlagh*, Hassan Abolhassani, Asghar Aghamohammadi

Journal Name: Endocrine, Metabolic & Immune Disorders - Drug Targets
Formerly Current Drug Targets - Immune, Endocrine & Metabolic Disorders

Become EABM
Become Reviewer
Call for Editor


Kabuki syndrome is a rare congenital anomaly/mental retardation syndrome characterized by intellectual disability, developmental delay, short stature, facial dysmorphic features including ectropion of the lateral third of the lower eyelids and long palpebral fissures, and prominent finger pads. Pathogenic variants of KMT2D (MLL2) and KDM6A are found to be the major causes of Kabuki syndrome. Here, we report the first Iranian case with Kabuki syndrome with an IQ of 79, two episodes of viral pneumonia and distinctive facial features, prominent ears and persistent fetal fingertip pads. These characteristics raised our suspicion for performing whole-exome sequencing (WES), which revealed 2 heterozygous pathogenic missense variants in the KMT2D gene: c.C10024T in exon 34 leading to p.R3342C and c.G15005A in exon 48 leading to p.R5002Q. Hence, the definitive diagnosis of Kabuki syndrome was made based on molecular findings along with the intellectual disability and characteristic facial features.

Keywords: Primary immunodeficiency, Kabuki syndrome, KMT2D, mental retardation, facial dysmorphic features, case report

Rights & PermissionsPrintExport Cite as

Article Details

Published on: 14 January, 2021
(E-pub Ahead of Print)
DOI: 10.2174/1871530321666210114153920
Price: $95

Article Metrics

PDF: 194