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Simultaneous corrective osteotomy and fracture fixation in a patient with polydactyly

Kim YH, Gu JH

No abstract available.
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Clinical Study of 31 Polydactyly Cases Admitted to Neonatal Intensive Care Unit

Lee Y, Gang M, Chang M, Song W, Kim S

OBJECTIVE: To investigate polydactyly in neonates who were admitted to neonatal intensive care unit (NICU) due to urgent medical needs. METHODS: Retrospective chart review of polydactyly neonates admitted to NICU of...
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Analysis of Congenital Postaxial Polydactyly of the Foot Using Magnetic Resonance Imagings

Woo SH, Baek HS, Kim YK, Choi JY

PURPOSE: We aimed to evaluate the magnetic resonance imaging (MRI) findings of congenital postaxial polydactyly of the foot. MATERIALS AND METHODS: Three-hundred and forty-seven feet of 288 patients who underwent congenital...
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A Case of Rudimentary Polydactyly: Is It Truly Related to Polydactyly?

Cheon SJ, Jin H, You HS, Shim WH, Kim JM, Kim GW, Kim HS, Ko HC, Kim BS, Kim MB

  • KMID: 2436670
  • Korean J Dermatol.
  • 2018 Mar;56(3):202-205.
Rudimentary polydactyly is a congenital anomaly of the hand clinically ranging from a small wart-like tumor to a pedunculated structure near the thumb or little finger. The histology reveals a...
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Surgical Treatment of Axial Polysyndactyly and Postaxial Polydactyly of The Hand in Korean: A Clinical Analysis of 24 Cases

Kim BJ, Choi JH, Kwon ST

PURPOSE: Non-preaxial polydactyly of the hand refers to axial polysyndactyly involving the 2nd, 3rd, or 4th finger and postaxial polydactyly involving the 5th finger. It has a much lower incidence...
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Postaxial Polydactyly of the Hands and Feet in Monozygotic Twins

Hwang SM, Park B, Hwang MK, Kim HD, Kim MW, Lee JS

Polydactyly is the most common congenital difference of the hand and foot presenting as a range of defects from minor soft tissue duplications to major bony abnormalities. Although polydactyly of...
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Identification of Two Cases of Ciliopathy-Associated Diabetes and Their Mutation Analysis Using Whole Exome Sequencing

Kim MK, Kwak SH, Kang S, Jung HS, Cho YM, Kim SY, Park KS

BACKGROUND: Alstrom syndrome and Bardet-Biedl syndrome are autosomal recessively inherited ciliopathies with common characteristics of obesity, diabetes, and blindness. Alstrom syndrome is caused by a mutation in the ALMS1 gene,...
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Variable expression observed in a Korean family with Townes-Brocks syndrome caused by a SALL1 mutation

Seo YJ, Lee KE, Ko JM, Kim GH, Yoo HW

Townes-Brocks syndrome (TBS) is a rare genetic disorder characterized by the classic triad of congenital anomalies of the anus, thumbs, and ears, with variable expressivity. Additionally, renal malformations, cardiac anomalies,...
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A Case of Langer-Giedion Syndrome with a De Novo Del(8)(q23q24.1)

Lee JM, Lee SB, Lee SW, Shim SY, Cho SJ, Park EA, Huh JW

Lange-Giedion syndrome, or trichorhinophalangeal syndrome type 2 (TRPSII), is a clinical syndrome characterized by mild growth restriction, mental retardation, microcephaly and dysmorphic face. Bulbous nose, large protruding ears and loose...
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Prenatal diagnosis of a 7q21.13q22.1 deletion detected using high-resolution microarray

Kim KB, Ha JS, Shin SJ, Kim CS, Bae JG

We report a case of de novo 7q interstitial deletion detected by conventional karyotyping and by microarray of amniotic fluid sampled during the prenatal period. A 32-year-old pregnant woman was...
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A chromosome 1q44 deletion in a 4-month-old girl; The first report in Korea

Cho JH, Song ES, Kim HN, Oh BS, Choi YY

The deletion of the distal long arm of chromosome 1 is associated with a characteristic facial appearance and a pattern of associated malformations. Characteristic manifestations include a round face with...
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Two siblings with Bardet-Biedl syndrome caused by mutations in BBS10: the first case identified in Korea

Yoon SC, Lee HJ, Ko JM, Kang HG, Cheong HI, Yu HG, Kim JH

Bardet-Biedl syndrome (BBS) is a rare ciliopathy generally inherited with an autosomal recessive pattern. BBS is characterized by 6 primary features namely retinal dystrophy, obesity, postaxial polydactyly, renal dysfunction, learning...
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Acromegaloid Facial Appearance Syndrome: A New Case in India

Rai A, Sattur AP, Naikmasur

Acromegaloid Facial Appearance syndrome is a very rare syndrome combining acromegaloid-like facial appearance, thickened lips and oral mucosa and acral enlargement. Progressive facial dysmorphism is characterized by a coarse facies,...
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New Classification of Polydactyly of the Foot on the Basis of Syndactylism, Axis Deviation, and Metatarsal Extent of Extra Digit

Seok HH, Park JU, Kwon ST

BACKGROUND: Polydactyly of the foot is one of the most frequent anomalies of the limbs. However, most classification systems are based solely on morphology and tend to be inaccurate and...
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Changing Patterns of Congenital Anomalies over Ten Years in a Single Neonatal Intensive Care Unit

Chung SH, Kim HY, Kim JH, Choi YS, Lee BS, Kim KS, Kim EA

PURPOSE: To investigate incidence, changing patterns, and mortality associated with congenital anomalies experienced in a single neonatal intensive care unit (NICU). METHODS: Retrospective chart review of 29,026 neonates admitted to NICU...
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Treatment of Congenital toe Anomalies

Cha SM, Suh JS

  • KMID: 2181694
  • J Korean Foot Ankle Soc.
  • 2012 Sep;16(3):148-155.
There are many different type of congenital toe anomalies such as syndactyly, polydactyly which are more common, and less frequently macrodactyly and curly toe. Congenital anomaly of hand can decrease...
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Antenatal sonographic features of intestinal neuronal dysplasia type A associated with polydactyly and micromelia

Son HJ, Jo YS, Jung JH, Jang DG, Lee G

Type A intestinal neuronal dysplasia is a congenital abnormality that is a very rare disease. Here, we report on a patient who had intestinal dilatation with serial changes and polydactyly,...
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Patient Characteristics and Treatment of Hallux Polydactyly Associated with Varus Deformity

Ro DH, Chung MS, Baek GH, Lee HJ, Song CH, Kim H, Gong HS

PURPOSE: To evaluate patient characteristics such as deformity type, associated disease, and family history, and results of treatment of pre-axial polydactyly with hallux varus deformity. MATERIALS AND METHODS: We carried out...
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Ellis-van Creveld syndrome in an Indian child: a case report

Veena KM, Jagadishchandra H, Rao PK, Chatra L

Ellis-van Creveld syndrome is a rare congenital genetic disorder having autosomal recessive inheritance. It is a syndrome affecting the Amish population of Pennsylvania in USA with prevalence rate of 1/5,000...
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A case of McKusick-Kaufman syndrome

Son SH, Kim YJ, Kim ES, Kim EK, Kim HS, Kim BI, Choi JH

McKusick-Kaufman syndrome (MKS) is an autosomal recessive multiple malformation syndrome characterized by hydrometrocolpos (HMC) and postaxial polydactyly (PAP). We report a case of a female child with MKS who was...
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