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진료과안내

소아청소년과

이정현 사진
Kosin University Gospel Hospital
소아청소년과   이정현

진료과

소아청소년과

 

전문진료분야

성장클리닉(성조숙증, 저신장), 내분비대사질환(고신장, 사춘기 지연, 갑상선질환, 당뇨병, 저혈당, 비만, 칼슘 및 인 대사 장애, 기타 영양 장애)

 

약력

[학력사항]
고신대학교 의과대학 의학사
고신대학교 의과대학 의학석사
고신대학교 의과대학 의학박사

[교육 및 연구경력]
고신대학교복음병원 수련의
고신대학교복음병원 소아청소년과 전공의
서울아산병원 소아내분비유전대사분과 전임의
고신대학교의과대학 소아과학교실 전임강사
고신대학교의과대학 소아과학교실 조교수
고신대학교의과대학 임상교육지원실장
현 고신대학교의과대학 소아과학교실 부교수

[면허/자격]
의사면허
소아청소년과 전문의 자격
소아청소년 내분비 세분전문의 자격

 

Updated date : 2020.10.21

학회활동 및 논문

[학회활동]
대한소아청소년과학회 정회원
대한소아내분비학회 정회원
대한소아내분비학회 보험위원
대한유전성대사질환학회 정회원
대한의학유전학회 정회원
대한당뇨병학회 정회원
대한비만학회 평생회원
대한내분비학회 평생회원
대한소아소화기영양학회 평생회원
전 부산소아청소년과학회 학술이사
전 서라벌학회 연제선정 위원

[수상]
2006 대한소아과학회 추계학술대회 GSK우수초록상
2007 서울아산병원장 표창
2012 젊은 연구자상 (ASPR, 아시아소아과연구학회)
2020 보원(普園)학술논문상(대한소아청소년과학회)

[출판된 책]
희귀난치성질환의 이해 IX (공저) 희귀난치성질환 총서 35-51
희귀난치성질환의 이해 XI (공저) 희귀난치성질환 총서 55-65
알면 알수록 건강해지는 제1형 당뇨병 안내서 (공저) 부산당뇨병캠프

[논문]
Parental anxiety regarding premature infants and factors affecting parental concern. J Spec Pediatr Nurs. 2019;24:e12266.

Pevalence of hyperuricemia and its association with metabolic syndrome and cardiometabolic risk factors in Korean children and adolescents: based on the 2016-2017 Korea National Health and Nutrition Examination Survey. Korean J Pediatr. 2019;62:317-23.

The Effect of Delayed Elevation of Thyrotropin on Feeding Intolerance in Very Low Birth Weight Infants. Neonatal Medicine. 2019;26:102-10.

Blood lead concentrations and attention deficit hyperactivity disorder in Korean children: a hospital-based case control study. BMC Pediatr. 2016;16:156.

Incidence trends and associated factors of diabetes mellitus in Korean children and adolescents: a retrospective cohort study in Busan and Gyeongnam. Ann Pediatr Endocrinol Metab. 2015;20:206-12.

Preterm Ovarian Hyperstimulation Syndrome. Neonatal Medicine. 2015;22:223-7

Psychological Characteristics and Attention of Children with Short Stature : Multicenter, Case-control Study. J Korean Soc Biol Ther Psychiatry. 2015;21:174-80.

Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiency. J Hum Genet. 2015;60:501-7

OTC gene in ornithine transcarbamylase deficiency: clinical course and mutational spectrum in seven Korean patients. Pediatr Neurol. 2014;51:354-9

Dietary patterns in children with attention deficit/hyperactivity disorder (ADHD). Nutrients. 2014;6:1539-53.

Severe dapsone hypersensitivity syndrome in a child. Korean J Pediatr. 2013;56:260-4.

The Study in Vitamin D Concentration in the Blood for Infants with High Level of Alkaline Phosphatase. Kosin Med J. 2012;27:17-24.

Assessment of Iron Parameters in Children with Acute Infectious Disease. Clin Pediatr Hematol Oncol. 2012;19:72-7.

High allele frequency of the p.Q258X mutation and identification of a novel mis-splicing mutation in the STAR gene in Korean patients with congenital lipoid adrenal hyperplasia. Eur J Endocrinol. 2011;165:771-8.

Clinical characterization and identification of two novel mutations of the GNAS gene in patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism. Clin Endocrinol (Oxf). 2011;75:207-13.

A 9-month-old phosphaturic mesenchymal tumor mimicking the intractable rickets. J Pediatr Orthop B. 2010;19:127-32.

Effects of Family Environment and Parenting Behavior on Glycemic Control and Depressive Symptoms in Children with Type 1 Diabetes. J Korean Soc Pediatr Endocrinol. 2009;14:100-109.

Growth Assessment of Children and Adolescents Complaining of Short Stature. Kosin Med J. 2008;23:42-8.

Long-term Follow-up Outcome in Children and Adolescents with Hashimoto's Thyroiditis. J Korean Soc Pediatr Endocrinol. 2008;13:163-72.

A Case of Achodroplasia Confirmed by Mutation Analysis of FGFR3 Gene. Kosin Med J. 2008;23:90-4.

A Case of Prader-Willi Syndrome with Hypotonia and Cryptorchidism Diagnosed at Neonate. Kosin Med J. 2007;22:186-90.

A case of a Korean newborn with IMAGe association presenting with hyperpigmented skin at birth. Eur J Pediatr. 2007;166:879-80.

AGL gene mutation and clinical features in Korean patients with glycogen storage disease type III. Journal of the Korean Society of Inherited Metabolic Disease 2006;6:15-23.

Clinical Characteristics of Type 2 Diabetes in Children and Adolescents. J Korean Soc Pediatr Endocrinol. 2006;11:64-9.

Clinical Course and Outcome Thyroid Carcinoma in Childhood. J Korean Soc Pediatr Endocrinol. 2006;11:57-63.

A case of Propionic Acidemia with Gait Disturbance. Journal of the Korean Society of Inherited Metabolic Disease 2006;6:6-14.

Paternity Test by Analysis of HLA Antigens. Kosin Med J. 2006;21:133-8.

A Case of Rothmund-Thomson Syndrome with Pure Red Cell Aplasia, Autoimmune Hemolytic Anemia and Chronic Respiratory Infection. Korean J Pediatr. 2004;47:1351-5.

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