Chong Kun Cheon

Associate Professor

Pusan National University School of Medicine

South Korea

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Research Interests

Internal Medicine

60%

Pediatric Nutrition

80%

Rare Disease

90%

Medical Science

80%

Endocrinology

50%

Pediatric Endocrinology

40%

Osteogenesis Imperfecta

30%

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Articles17

The impacts of COVID-19 on childhood obesity: prevalence, contributing factors, and implications for management

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Year:

2024

The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome

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Year:

2024

NANS‐CDG: Expanding clinical insights with a novel patient with novel variants

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Year:

2024

Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency

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Year:

2024

A novel compound heterozygous variant of the COL11A1 gene in a patient with fibrochondrogenesis type I: the first case in Korea

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Year:

2024

A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish

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Year:

2023

Pediatric management challenges of hyperglycemic hyperosmolar state: case series of Korean adolescents with type 2 diabetes

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Year:

2023

The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea

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Year:

2023

Haploinsufficiency A20 misdiagnosed as PFAPA (periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis) syndrome with Kikuchi disease

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Year:

2023

A Korean child with DICER1 syndrome presenting with thyroid manifestations accompanied by other types of neoplasms: a case report and literature review

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Year:

2023

Commentary on "Glycemic control and complications of type 2 diabetes mellitus in children and adolescents during the COVID-19 outbreak"

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Year:

2023

Prospective evaluation of the clinical utility of whole-exome sequencing using buccal swabbing for undiagnosed rare diseases

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Year:

2022

From diagnosis to treatment of mucopolysaccharidosis type VI: A case report with a novel variant, c.1157C>T (p.Ser386Phe), in ARSB gene

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Year:

2022

Response to growth hormone according to provocation test results in idiopathic short stature and idiopathic growth hormone deficiency

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Year:

2022

Fabry nephropathy before and after enzyme replacement therapy: important role of renal biopsy in patients with Fabry disease

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Year:

2021

Commentary on "Effects of gonadotropin-releasing hormone agonist treatment on final adult height in boys with idiopathic central precocious puberty"

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Year:

2021

Clinical relevance of targeted exome sequencing in patients with rare syndromic short stature

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Year:

2021