Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

19 results
Display

Signature Genes in Macrodactyly through Transcriptome Network Analysis Reveal their Association of Lipid Metabolism

Choi JW, Lee HJ, Oh JW

Macrodactyly is one of the most difficult hand anomalies to treat not only surgically but medically as well. Little is known about the molecular pathways and lipid metabolism of this...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Gigantism caused by growth hormone secreting pituitary adenoma

Rhee N, Jeong K, Yang EM, Kim CJ

Gigantism indicates excessive secretion of growth hormones (GH) during childhood when open epiphyseal growth plates allow for excessive linear growth. Case one involved a 14.7-year-old boy presented with extreme tall...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Radiologic Imaging Findings of Bilateral Infiltrating Pseudoangiomatous Stromal Hyperplasia of the Breasts: A Case Report

Go HS, Jeh SK

Pseudoangiomatous stromal hyperplasia (PASH), first described by Vuitch et al., is a rare benign lesion, shows the proliferation of the breast stromal tissue. We experienced a case of a 19-year-old...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Klinefelter Syndrome Differentially Diagnosed as a Cause of Gigantism

Kim JY, Choi YJ, Rhee SY

  • KMID: 2259004
  • Korean J Med.
  • 2011 Mar;80(3):343-347.
Klinefelter syndrome is a congenital disease that is associated with the existence of an extra X chromosome, and is one of the most common causes of male primary hypogonadism. In...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Management of Proteus Syndrome with Craniofacial Hemihyperostosis: Case Report

Yun YE, Seol KY, Oh MS, Choi JG, Kim SJ, Lee DK, Kang JY

  • KMID: 2136938
  • J Korean Assoc Maxillofac Plast Reconstr Surg.
  • 2011 Nov;33(6):540-548.
Proteus syndrome is a congenital hamartomatous malformation that is characterized by a wide range of deformities, including craniofacial deformities. Proteus syndrome features partial gigantism and asymmetry of the limbs, plantar...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of Breast Gigantism in a Patient with Wilson's Disease treated by Penicillamine

Lee JE, Shin HJ, Hwang SE, Hwang KT, Oh SK, Youn YK, Noh DY, Kim SW, Han W

We report a case of breast gigantism in a patient with Wilson's disease treated with penicillamine. A 19-year-old female with alleged Wilson's disease visited our hospital due to diffuse enlargement...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Reduction glossectomy of macroglossia in beckwith-wiedemann syndrome : a case report

Kim HK, Kim ES, Ko YK, Kim SG

  • KMID: 1575609
  • J Korean Assoc Maxillofac Plast Reconstr Surg.
  • 2005 Nov;27(6):559-564.
Beckwith-Wiedemann syndrome is an autosomal dominant growth excess disorder, which occurs with a reported incidence of 1 in 13,700 to 1 in 17,000 live births. It constitutes a discrete...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Isolated Familial Somatotropinoma

Park HR, Kim EA, Jiang MH, Jang CS, Lee KW, Hong SB, Kim EY, Lim MK, Nam MS, Kim YS

  • KMID: 2200527
  • J Korean Soc Endocrinol.
  • 2004 Aug;19(4):398-405.
The familial occurrence of a pituitary adenoma associated with multiple endocrine neoplasia (MEN) type 1 or Carney complex is a well-recognized entity. However, an isolated familial somatotropinoma is a rare...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Breast Gigantism Induced by D-Penicillamine: Case Report

Cha JH, Kim HH, Kim SM, Seo MH, Yoon HS

D-penicillamine, a chelating agent of copper, is the drug of choice for the treatment of Wilson's disease. Breast enlargement is a rare complication arising from its use, and we report...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of acromegaly associated with moyamoya disease, coronary arterial stenosis, and dilated cardiomyopathy

Lee DH, Kim YJ, Lee DB, Park JH, Chung DJ, Chung MY, Lee TH

  • KMID: 2306240
  • Korean J Med.
  • 2000 Feb;58(2):227-233.
A 19-year-old girl with typical features of acromegaly, duration of which was thought to be above 10 years, presented with dyspnea. After serial studies, dilated cardiomyopathy and critical stenosis of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A CASE OF TONGUE RESECTION IN MACROGLOSSIA AS A PRESENTATION OF BECKWITH-WIEDEMANN SYNDROME

Ahn KY, Jang KS, Park DH, Hwang JB

  • KMID: 2119323
  • J Korean Soc Plast Reconstr Surg.
  • 1997 Jan;24(1):199-204.
The Beckwith-Wiedemann syndrome, originally described by Beckwith in 1963 and Wiedemann in 1964, included congenital anomalies such as macroglossia, exomphalos, postnatal somatic gigantism, severe hypoglycemia, abdominal wall defect, capillary nevus...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Testicular Yolk Sac Tumor in Beckwith-Wiedemann Syndrome

Park BJ, Jeong IY, Ro DW, Kim DY, Park JS

  • KMID: 1663291
  • Korean J Urol.
  • 1996 Dec;37(12):1417-1420.
The Beckwith-Wiedemann syndrome, which included congenital anomalies such as macroglossia, exomphalos, postnatal somatic gigantism, have a substantially increased risk for the development of tumor. We report a case of testicular...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Klippel-trenaunay-weber syndrome

Ryu KN, Lee SW, Yoon Y, Lim JH

The Klippel-Trenaunay-Weber syndrome is characterized by a classical triad that includes unilateral cutaneouscapillary hemangiomas, varicose veins, and local gigantism with both soft tissue and osseous overgrowth. Authorshave experienced one case...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Scoliosis in Neurofibromatosis

Suk SI, Song HS, Chang JS

Neurofibromatosis is a disease which involves both neuroectodermal and mesodermal tissue, and is characterized by cafe-au-lait spot, multiple subcutaneous neurofibromas, elephantiasis neuromatosa, a positive family history, and specific dystrophic osseous...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Beckwith Syndrome

Kim KT, Hong DS, Nam BD, Kim KT

  • KMID: 1946088
  • J Korean Pediatr Soc.
  • 1981 Jul;24(7):696-698.
We experienced one case of Beckwith syndrome. This one day aged male neonate manifested macroglossia, umbilical hernia, visceromegaly, hypoglycemia, gigantism and polycythemia. A brief review of related literature is also...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Hypertrophy of an Extremity Associated with Neurofibromatosis of the Sural Nerve: Report of one case

Kim ID, Lee SY, Ihin JC, Park YC

Overgrowth and hypertrophy of one or more extremities is an infrequentIy encountered congenital or acguired anomaly, It is referred to in the literature by different authors as local gigantism, hypertrophy...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Microsurgical Transsphenoidal Approach for Pituitary Denomas

Hahn YS, Lee HJ

  • KMID: 2106967
  • J Korean Neurosurg Soc.
  • 1976 Oct;5(2):195-208.
3 cases of pituitary adenomas, two hormone-secreting adenomas, and one non-secreting chromophobe adenoma, were treated surgically by the sublabial transsphenoidal approach with use of surgical microscope and radiofluroscopic image intensification...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Primary hyperparathyroidism erosion of the sternal ends of the clavicles, a new sign of hyperparathy...

Chae IW, Rhee BC

A Radiological analysis was made of 13 cases of confirmed acromegaly and gigantism. And observation was madein skeleton and soft tissue of patients at Yonsei university from 1968 to 1973....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Macrodactyly

Jung M, Chung CH

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of digit or digits. The phalanges, tendons, nerves, vessels, subcutaneous fat,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr