- Donor site morbidities of concha cartilage harvesting using a retroauricular approach for cleft rhinoplasty: retrospective study
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Themkumkwun S, Vorakulpipat C, Boonsiriseth K
- KMID: 2547571
- J Korean Assoc Oral Maxillofac Surg.
- 2023 Oct;49(5):270-277.
- doi: 10.5125/jkaoms.2023.49.5.270
Objectives: Concha cartilage is recommended for correction of cleft nasal deformities. Morbidities at the donor site have been reported in esthetic rhinoplasty cases. Reports on cleft patients are limited, so... -
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- A Case of Perineal Hemangioma, External Genitalia Malformations, Lipomyelomeningocele, Vesicorenal Abnormalities, Imperforate Anus, and Skin Tag (PELVIS) Syndrome with Extensive Perineal Infantile Hemangioma
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Hwang HW, Lee SB, Shin J, Choi GS, Byun JW
- KMID: 2542748
- Ann Dermatol.
- 2023 May;35(Suppl1):S88-S92.
- doi: 10.5021/ad.21.183
PELVIS syndrome describes the constellation of perineal hemangioma, external genitalia malformations, lipomyelomeningocele, vesicorenal abnormalities, imperforate anus, and skin tag. A 2-month-old girl presented with infantile hemangioma on her perineum and... -
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- Duplicated extrahepatic bile duct (type Vb): An important rare anomaly
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Varshney VK, Hussain S, Vignesh N, Selvakumar B, Agarwal L, Yadav T
- KMID: 2542588
- Ann Hepatobiliary Pancreat Surg.
- 2023 May;27(2):220-225.
- doi: 10.14701/ahbps.22-118
Congenital duplication of the extrahepatic bile duct (DEBD) is an unusual anomaly of the biliary system. It occurs due to inability of the embryological duplex biliary system to regress. DEBD... -
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- A Case of Patau Syndrome with Congenital Ocular Anomalies
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Ji M, Lee HJ, Jeong JH
- KMID: 2540671
- Ann Optom Contact Lens.
- 2023 Mar;22(1):37-41.
- doi: 10.52725/aocl.2023.22.1.37
Purpose: We report a case of bilateral congenital ocular anomaly in a patient with trisomy 13. Case summary: A newborn born with a gestational period of 38 weeks was transferred to... -
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- Fetal arachnoid cyst: characteristics, management in pregnancy, and neurodevelopmental outcomes
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Hong S, Pae J, Ko HS
- KMID: 2540473
- Obstet Gynecol Sci.
- 2023 Mar;66(2):49-57.
- doi: 10.5468/ogs.22113
Arachnoid cysts are rarely found during the prenatal period and can exist in any part of the brain as extra-axial cysts. These cysts are usually found after the second trimester... -
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- Perineal Groove: A Case Report and Re view of Literature
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Park S, Kim D, Oh JY, Lee J
- KMID: 2537727
- Perinatology.
- 2022 Dec;33(4):213-217.
- doi: 10.14734/PN.2022.33.4.213
Perineal groove is an uncommon congenital malformation of the nonepithelialized perineal mucous membrane, usually affecting female patients. It is not well known to many clinicians, and thus can be missed... -
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- Cervical chondrocutaneous remnant: a case report
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Park DH, Lee JK, Baik BS, Yang WS, Kim SY
- KMID: 2535764
- Arch Craniofac Surg.
- 2022 Oct;23(5):241-245.
- doi: 10.7181/acfs.2022.00920
Cervical chondrocutaneous branchial remnants are very rare congenital lesions of the lateral neck; thus, our knowledge of this condition derives almost entirely from occasional case reports in the literature. They... -
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- Aortic Arch Variants and Anomalies: Embryology, Imaging Findings, and Clinical Considerations
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Bae SB, Kang EJ, Choo KS, Lee J, Kim SH, Lim KJ, Kwon H
- KMID: 2534489
- J Cardiovasc Imaging.
- 2022 Oct;30(4):231-262.
- doi: 10.4250/jcvi.2022.0058
There is a wide spectrum of congenital anomalies or variations of the aortic arch, ranging from non-symptomatic variations that are mostly detected incidentally to clinically symptomatic variations that cause severe... -
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- Correction of pixie ear: infraauricular skin redraping method
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Kim JH, Yang YB, Oh DY
- KMID: 2532962
- Arch Craniofac Surg.
- 2022 Aug;23(4):187-189.
- doi: 10.7181/acfs.2022.00675
Patients with pixie ear have an attached, tapering, and low-set earlobe. Traditional methods usually describe excision of the caudal portion of the lobule and reattachment in a more superior position.... -
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- Acute Myocardial Infarction in Patients With Single Coronary Artery: A Case Report
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Thi HN, Ngoc TN, Khoi VN, Thuy LLT, Van HHT, Bao NP, Dang LV
- KMID: 2529411
- Cardiovasc Imaging Asia.
- 2022 Apr;6(2):49-52.
- doi: 10.22468/cvia.2021.00325
A single coronary artery (SCA) is a rare congenital anomaly. In most cases, it is an incidental finding on coronary angiography and has no clinical significance. However, it can cause... -
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- Neonatal Duodenal Obstruction Associated with Situs Inversus Totalis: A Case Report
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Seo J, Kim YJ, Ho YH
- KMID: 2527756
- Perinatology.
- 2022 Mar;33(1):43-47.
- doi: 10.14734/PN.2022.33.1.43
Situs inversus totalis is a mirror reversal of the normal asymmetrical arrangement of the viscera. The incidence is approximately 0.3 in 10,000 live births. Situs inversus totalis is commonly seen... -
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- Pregnancy and neonatal outcomes after periconceptional exposure to isotretinoin in Koreans
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Cha EH, Kim N, Kwak HS, Han HJ, Joo SH, Choi JS, Chun KC, Kim YA, Koh JW, Han JY
- KMID: 2527268
- Obstet Gynecol Sci.
- 2022 Mar;65(2):166-175.
- doi: 10.5468/ogs.21354
Objective Isotretinoin should not be used during pregnancy because of the risk of birth defects. Most pregnant women exposed to isotretinoin choose voluntary pregnancy termination due to concerns about birth defects.... -
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- Cochlear Implants for Patients With Common Cavity Deformities and the Impact of Electrode Positioning
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Bae SH, Choi J, Choi JY
- KMID: 2527115
- Clin Exp Otorhinolaryngol.
- 2022 Feb;15(1):77-83.
- doi: 10.21053/ceo.2021.00745
Objectives. Common cavity deformity is a rare congenital bony labyrinth malformation associated with profound hearing loss. Cochlear implants are widely used for hearing rehabilitation for common cavity deformities; however, the... -
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- Trends and Characteristics of Mortality Associated with Congenital Anomalies in Korean Children under 5 Years of Age
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Kim SB, Jang MJ, Song YH, Jung SY, Oh JS, Lim JW
- KMID: 2519772
- Neonatal Med.
- 2021 Aug;28(3):99-107.
- doi: 10.5385/nm.2021.28.3.99
Purpose: Studies have been conducted on the prevalence and infant mortality rate of congenital anomalies; however, studies on child mortality are rare. Therefore, we evaluated the characteristics of deaths associated... -
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- Potential Implications of Slim Modiolar Electrodes for Severely Malformed Cochleae: A Comparison With the Straight Array With Circumferential Electrodes
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Lee SY, Choi BY
- KMID: 2519183
- Clin Exp Otorhinolaryngol.
- 2021 Aug;14(3):287-294.
- doi: 10.21053/ceo.2021.00752
Objectives. Malformations of the inner ear account for approximately 20% of cases of congenital deafness. In current practice, straight arrays with circumferential electrodes (i.e., full-banded electrodes) are widely used in... -
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- Angiographic Findings of an Isolated Meandering Pulmonary Vein: A Case Report
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Ko JS, Kwon LM, Kim HM, Woo JY, Kim YN, Moon JW
- KMID: 2518637
- J Korean Soc Radiol.
- 2021 Jul;82(4):1018-1023.
- doi: 10.3348/jksr.2020.0170
A meandering pulmonary vein (MPV) is a rare pulmonary vascular anomaly characterized by an abnormal course of the pulmonary vein draining into the left atrium. We report the case of... -
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- A Case of Coronary Sinus Atresia with a Total Anomalous Cardiac Venous Drainage to the Left Atrium without Persistent Left Superior Vena Cava: Imaging Findings on Cardiac CT
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Baek SH, Kang EJ, Lee KN
- KMID: 2518631
- J Korean Soc Radiol.
- 2021 Jul;82(4):982-987.
- doi: 10.3348/jksr.2020.0104
The coronary sinus (CS) is the venous drainage system of the heart. CS ostium atresia is a rarely seen cardiac malformation. Congenital atresia of the CS is usually found together... -
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- Trisomy 9 Mosaicism in an Extremely Low Birth Weight Infant
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Cho H, Heo JS, Ahn KH, Hong SC
- KMID: 2522524
- Perinatology.
- 2021 Jun;32(2):100-103.
- doi: 10.14734/PN.2021.32.2.100
Trisomy 9 mosaicism is a rare chromosomal abnormality with distinct and recognizable clinical features. In this report, we present an extremely low birth weight (ELBW) infant with trisomy 9 mosaicism.... -
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- The first Korean case of a newborn with 3p26 microdeletion and 5q35 microduplication inherited from paternal balanced translocation
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Jang JA, Sohn YB, Lee JH, Park MS
- KMID: 2517212
- J Genet Med.
- 2021 Jun;18(1):48-54.
- doi: 10.5734/JGM.2021.18.1.48
Genetic imbalances are a major cause of congenital and developmental abnormalities. We report the first case of a 3p26 microdeletion and 5q35.2q35.3 microduplication in a newborn with multiple congenital anomalies... -
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- Antithyroid Drug Treatment in Graves’ Disease
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Chung JH
- KMID: 2517638
- Endocrinol Metab.
- 2021 Jun;36(3):491-499.
- doi: 10.3803/EnM.2021.1070
Graves’ disease is associated with thyrotropin (TSH) receptor stimulating antibody, for which there is no therapeutic agent. This disease is currently treated through inhibition of thyroid hormone synthesis or destruction... -
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