Chong Kun Cheon

Associate Professor

Pusan National University School of Medicine

South Korea

Research Interests

Explore related searches

Professors in South Korea Professors in Medical Science Medical Science professors in South Korea

About

Chong Kun Cheon is an Associate Professor at Pusan National University School of Medicine in South Korea. His research focuses on rare diseases and metabolic disorders, with recent publications addressing topics such as multidisciplinary care models, cohort studies for pediatric endocrine diseases, and innovative genetic mutations related to various conditions. His work also examines the impacts of COVID-19 on childhood obesity and other health implications in the pediatric population.

Articles (22)

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

SOUTH KOREA

View details

Il Young Kim

Pusan National University Yangsan Hospital

SOUTH KOREA

View details

Su Eun Park

Pusan National University Yangsan Hospital

SOUTH KOREA

View details

Yong Hee Hong

SOUTH KOREA

View details

Yoo-Mi Kim

Pusan National University Yangsan Hospital

SOUTH KOREA

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Chong Kun Cheon

Research Interests

Explore related searches

About

Articles (22)

「찾아가는 희귀질환 진단지원 사업」 성과와 기대

Multidisciplinary Care Model as a Center of Excellence for Fabry Disease: A Practical Guide to Diagnosis and Management by Clinical Specialty in South Korea

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

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

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

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

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

Cohort profile: Multicenter Networks for Ideal Outcomes of Rare Pediatric Endocrine and Metabolic Diseases in Korea (OUTSPREAD study).

Molecular and clinical delineation of patients with fatty acid oxidation disorder: A single center’s experience

Commentary on "Deciphering the mystery of CHNG3"

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

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

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

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

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

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

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

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

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

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

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

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

Collaborators (9)

YongBeom Shin

Hyun Jung Lee

Han Hyuk Lim

Seung Hwan Oh

Ju Young Yoon

Il Young Kim

Su Eun Park

Yong Hee Hong

Yoo-Mi Kim

Make your next move.

Chong Kun Cheon

Research Interests

Explore related searches

About

Articles (22)

「찾아가는 희귀질환 진단지원 사업」 성과와 기대

Multidisciplinary Care Model as a Center of Excellence for Fabry Disease: A Practical Guide to Diagnosis and Management by Clinical Specialty in South Korea

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

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

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

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

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

Cohort profile: Multicenter Networks for Ideal Outcomes of Rare Pediatric Endocrine and Metabolic Diseases in Korea (OUTSPREAD study).

Molecular and clinical delineation of patients with fatty acid oxidation disorder: A single center’s experience

Commentary on "Deciphering the mystery of CHNG3"

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

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

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

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

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

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

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

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

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

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

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

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

Collaborators (9)

YongBeom Shin

Hyun Jung Lee

Han Hyuk Lim

Seung Hwan Oh

Ju Young Yoon

Il Young Kim

Su Eun Park

Yong Hee Hong

Yoo-Mi Kim

Make your next move.

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