• 대한생식의학회:학술대회논문집
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• 2007.11a
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• pp.137-137
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• 2007

• 대한생식의학회:학술대회논문집
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• 2006.06a
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• pp.155.1-155.1
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• 2006

• 대한생식의학회:학술대회논문집
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• 1994.10a
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• pp.31.2-32
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• 1994

• 대한생식의학회:학술대회논문집
• /
• 2006.11a
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• pp.151-152
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• 2006

• 대한생식의학회:학술대회논문집
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• 2006.06a
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• pp.155.2-155.2
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• 2006

• 대한생식의학회:학술대회논문집
• /
• 2005.11a
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• pp.104-104
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• 2005

• 대한생식의학회:학술대회논문집
• /
• 2005.11a
• /
• pp.125-125
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• 2005

• 대한생식의학회:학술대회논문집
• /
• 2006.06a
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• pp.157.2-157.2
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• 2006

• Obstetrics & gynecology science
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• v.61 no.6
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• pp.702-706
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• 2018

A supernumerary ovary is a rare gynecological anomaly, and is usually excised due to its malignant transformation potential. We report a case of a supernumerary ovary and endometriosis situated on the anterior rectosigmoid colon. When laparoscopy was conducted, a firm, 5-cm mass was discovered on the anterior rectosigmoid colon along with normal ovaries. In this case, the discovery of a supernumerary ovary implied the presence of endometriosis. It is unusual for endometriosis and a supernumerary ovary to exist simultaneously.

• Journal of Genetic Medicine
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• v.12 no.2
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• pp.123-127
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• 2015

Distal limb deformities are congenital malformations with phenotypic variability and high genetic heterogeneity. Split hand/foot malformation, also known as ectrodactyly, is a congenital limb malformation characterized by a defect of the central rays of the hands and/or feet. Split hand/foot malformation with long-bone deficiency (SHFLD) is a rare condition related to a 17p13.3 duplication. Recently, genomic duplications encompassing BHLHA9 have been associated with SHFLD. We report a case of SHFLD presenting with campomelia of the right femur, bilateral agenesis of fibulae, bilateral club feet, and oligosyndactyly of the hands and feet, that was associated with a 17p13.3 duplication, as determined prenatally using array comparative genomic hybridization.