Further delineation of ERF-related Chitayat syndrome

Chitayat syndrome (CHYTS) is an autosomal dominant disorder caused by variants in the ETS2 repressor factor (ERF) gene, located on 19q13.2. This gene encodes the ERF protein. The syndrome is extremely rare, with only 13 patients reported to date. We present a patient of CHYTS resulting from a c.1201_1202del (p.Lys401Glufs∗10) frameshift variant in the ERF (NM_001429.3) gene. The patient, a 10-year-old girl, exhibited typical features of the syndrome such as short stature, facial dysmorphism, and early developmental delay. She was treated with recombinant human growth hormone for ∼5 years due to her short stature. During treatment, no complications such as increased intracranial pressure, hypothyroidism, or pancreatic dysfunction were noted. However, the growth response was suboptimal, with a total height increase of 25.4 cm. This patient provides valuable insights into the clinical manifestations and treatment outcomes associated with ERF(NM_001429.3) gene variants, contributing to the existing knowledge and potentially aiding clinicians in understanding similar patients.

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Publication Details

Journal
European Journal of Medical Genetics
Published
2025-08-20
DOI
https://doi.org/10.1016/j.ejmg.2025.105038
Primary Topic
Neurofibromatosis and Schwannoma Cases
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article
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article

Further delineation of ERF-related Chitayat syndrome

Chaochun Zou, Yu Zhang, Kaixuan Wang, Feng Zhu
European Journal of Medical Genetics
Neurofibromatosis and Schwannoma Cases
article

Further delineation of ERF-related Chitayat syndrome

Chaochun Zou, Yu Zhang, Kaixuan Wang, Feng Zhu
article en

Abstract

Chitayat syndrome (CHYTS) is an autosomal dominant disorder caused by variants in the ETS2 repressor factor (ERF) gene, located on 19q13.2. This gene encodes the ERF protein. The syndrome is extremely rare, with only 13 patients reported to date. We present a patient of CHYTS resulting from a c.1201_1202del (p.Lys401Glufs∗10) frameshift variant in the ERF (NM_001429.3) gene. The patient, a 10-year-old girl, exhibited typical features of the syndrome such as short stature, facial dysmorphism, and early developmental delay. She was treated with recombinant human growth hormone for ∼5 years due to her short stature. During treatment, no complications such as increased intracranial pressure, hypothyroidism, or pancreatic dysfunction were noted. However, the growth response was suboptimal, with a total height increase of 25.4 cm. This patient provides valuable insights into the clinical manifestations and treatment outcomes associated with ERF(NM_001429.3) gene variants, contributing to the existing knowledge and potentially aiding clinicians in understanding similar patients.

European Journal of Medical GeneticsVol. 77
Wenzhou Medical University (CN), Ruian People's Hospital (CN), Children's Hospital of Zhejiang University (CN), Jinhua Academy of Agricultural Sciences (CN), Guang Fu Hospital (CN), Wenzhou City People's Hospital (CN), Jinhua Central Hospital (CN)
Openalex Percentile: Top 69%
Neurofibromatosis and Schwannoma Cases
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Further delineation of ERF-related Chitayat syndrome — Chaochun Zou, Yu Zhang, et al. · European Journal of Medical Genetics (2025) | TGRS Research Map | TGRS