A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. Issue 4 (11th January 2023)

• Record Type: Journal Article
• Authors: Akalın, Akçahan; Şimşek‐Kiper, Pelin Özlem; Taşkıran, Ekim Z.; Karaosmanoğlu, Beren; Utine, Gülen Eda; Boduroğlu, Koray
• Is Part Of: American journal of medical genetics. Volume 191:Issue 4(2023)
• Page Start: 1119
• Page End: 1127
• Publication Date: 2023-01-11
• Subjects: consanguinity -- CRIPT -- exome sequencing -- primordial dwarfism; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.63120
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract: Primordial dwarfism (PD) is one of a highly heterogeneous group of disorders characterized by severe prenatal/postnatal growth restriction. Defects in various pathways such as DNA repair mechanism, impaired centrioles, abnormal IGF expression, and spliceosomal machinery may cause PD including Seckel syndrome, Silver–Russell syndrome. Microcephalic osteodysplastic primordial dwarfism (MOPD) types I/III, II, and Meier–Gorlin syndrome. In recent years with the wide application of exome sequencing (ES) in the field of PD, new genes involved in novel pathways causing new phenotypes have been identified. Pathogenic variants in CRIPT (MIM# 604594) encoding cysteine‐rich PDZ domain‐binding protein have recently been described in patients with PD with a unique phenotype. This phenotype is characterized by prenatal/postnatal growth restriction, facial dysmorphism, ocular abnormalities, and ectodermal findings such as skin lesions with hyper/hypopigmented patchy areas and hair abnormalities. To our knowledge, only three patients with homozygous or compound heterozygous variants in CRIPT have been reported so far. Here, we report on a male patient who presented with profound prenatal/postnatal growth restriction, developmental delay, dysmorphic facial features, and skin lesions along with the findings of bicytopenia and extensive retinal pigmentation defect. A novel truncating homozygous variant c.7_8delTG; p.(Cys3Argfs*4) was detected in CRIPT with the aid of ES. With this report, we further expand the mutational and clinical spectrum of this rare entity.