Intermittent macrothrombocytopenia in a novel patient with Takenouchi-Kosaki syndrome and review of literature.

Abstract

Takenouchi-Kosaki syndrome (TKS) is a recently delineated syndromic form of thrombocytopenia strictly related to an hot-spot missense variant, p.Tyr64Cys, in CDC42 (Cell Division Control protein 42). Herein we report an additional patient with the p.Tyr64Cys aminoacidic substitution who showed the well-defined phenotypical TKS features and an intermittent, very mild, macrothrombocytopenia at 10.7 years of age (93,000/mL), that was only retrospectively valorized. Outside of this value the PLT count had always been higher than 100,000/mL. We also review literature data from patients carrying this recurrent variant. Our female patient presented with prenatal onset of short stature and microcephaly, camptodactyly, heart defects, typical facial gestalt, developmental delay, and not specific brain abnormalities. After several genetic investigations (karyotype, CGH-Array, targeted NGS analysis for short stature genes), by whole exome sequencing we identified the p.Tyr64Cys in CDC42, occurring de novo. The case presented here provides further evidence that macrothrombocytopenia can be intermittent and thus it might escape attention of clinicians. Without this key feature, TKS clinical presentation can overlap other syndromic forms of short stature. Immunodeficiency, autoimmunity, and malignancies were recently reported in patients with the p.Tyr64Cys substitution, making imperative an early diagnosis of Takenouchi-Kosaki syndrome to organize the most proper follow-up of these pediatric patients. The whole exome sequencing can be a solving tool in the challenge to the rare diseases.

• Authors: Claudia Santoro, Giuseppina Gaudino, Annalaura Torella, Giulio Piluso, Silverio Perrotta, Emanuele Miraglia Del Giudice, Telethon Undiagnosed Diseases Program, Vincenzo Nigro, Anna Grandone
• Journal: European journal of medical genetics (Eur J Med Genet) Vol. 64 Issue 12 Pg. 104358 (Dec 2021) ISSN: 1878-0849 [Electronic] Netherlands
• PMID: 34624555 (Publication Type: Case Reports, Journal Article, Review)
• Copyright: Copyright © 2021 Elsevier Masson SAS. All rights reserved.

Topics

• Amino Acid Substitution (genetics)
• Child
• Female
• Humans
• Mutation, Missense (genetics)
• Phenotype
• Thrombocytopenia (genetics)