- A Case of Kallmann Syndrome and A Case of Successful Pregnancy of Kallmann Syndrome Patient
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Han SK, Kim JH, Park CS, Kim BC, Kim HS, Suh SS
- KMID: 2261992
- Korean J Obstet Gynecol.
- 2000 Jun;43(6):1088-1091.
Kallmann's syndrome is characterized by hypogonadotrophic hypogonadism resulting from insufficient release of GnRH and associated with anosmia or hyposmia, which has been related to agenesis of olfactory bulbs. We experienced a... -
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- Two Cases of Kallmann Syndrome
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Han HJ, Cho HJ, Lee HS, Lee IS, Hwang IT
- KMID: 1515008
- J Korean Soc Pediatr Endocrinol.
- 2003 Dec;8(2):179-183.
Kallmann syndrome is characterized by hypogonadotropic hypogonadism resulting from insufficient release of GnRH and associated with anosmia or hyposmia. We experienced two cases of Kallmann syndrome with abnormal brain MRI... -
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- Kallmann's syndrome associated with slipped capital femoralepiphysis: one case report
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Choy WS, Kim HJ, Lee KW, Park KH
- KMID: 2036090
- J Korean Orthop Assoc.
- 1991 Dec;26(6):1937-1943.
No abstract available. -
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- MR Findings of Kallmann Syndrome
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Kim SM, Choi JO, Lee KS, Choi SS
- KMID: 1945540
- J Korean Radiol Soc.
- 2000 Apr;42(4):601-604.
- doi: 10.3348/jkrs.2000.42.4.601
Kallman syndrome is characterised by hypogonadotrophic hypogonadism and anosmia. T1 weighted MR coronal images show the bilateral absence or hypoplasia of olfactory bulbs, tracts, and sulci. We report the MR... -
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- A Case of Kallmann's Syndrome: MR Imaging and Histopathology
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Yang KH, Lee CY, Park YM, Yu JM, Shim JW
- KMID: 2131706
- J Rhinol.
- 1998 May;5(1):63-67.
Kallmann's syndrome is a rare genetic disorder defined as a combination of anosmia or hyposmia and hypogonadism due to hypothalamic-pituitary deficiency. The incidence of Kallmann's syndrome is one in 100,000... -
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- A Case of Kallmann's Syndrome with Hypoplasia of Olfactory Bulb
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Nam YS, Lee SH, Han SY, Yoon TK, Cha KY
- KMID: 2235742
- Korean J Fertil Steril.
- 1999 Aug;26(2):281-285.
Kallmann's syndrome has both a general and specific connotation in describing general condition of gonadotropin-releasing hormone (GnRH) deficiency or a particular cluster of anomalies associated with primary eunuchoidism. The familial... -
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- A Case of Kallmann Syndrome Inherited in Autosomal Dominant Mode
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Nam YS, Lee SH, Lee WS, Park C, Kim JW, Cha KY
- KMID: 1891298
- Korean J Fertil Steril.
- 1999 Dec;26(3):491-495.
OBJECTIVE: To report the pedigree of Kallmann syndrome inherited in autosomal dominant mode with variable expressivity. MATERIAL AND METHOD: Case report. RESULTS: The patient had amenorrhea and anosmia but did not have... -
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- Two Cases of Kallmann Syndrome Presented with Delayed Puberty
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Choi HK, Choi JH, Yoo HW
- KMID: 2321985
- J Korean Soc Pediatr Endocrinol.
- 2005 Jun;10(1):105-109.
Kallmann syndrome is caused by the defects of migration of the olfactory and GnRH neurons from the olfactory placodes to the brain, and characterized by hypogonadotropic hypogonadism, and anosmia or... -
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- A Case of Kallmann's Syndrome Mildly Presenting as Secondary Amenorrhea
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Joo NR, Park CY, Moon HJ, Kang JG, Ihm SH, Choi MG, Yoo HJ, Lee Y, Oh KW, Park SW
- KMID: 1523094
- J Korean Endocr Soc.
- 2007 Apr;22(2):130-134.
- doi: 10.3803/jkes.2007.22.2.130
Kallmann's syndrome is very rare congenital defect in GnRH (gonadotrophin releasing hormone) secretion involving both sexes. The mode of inheritance has not been fully understood. But, including X-linked inheritance, the... -
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- A Case of Kallmann's Syndrome
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Lee IS, Kim JI, Chai SE
- KMID: 2289822
- Korean J Urol.
- 1985 Oct;26(5):549-551.
The association of anosmia with gonadal failure was first described by Kallmann et al. and reviewed by Nawakouski and Lenz. This hypogonadotropic hypogonadism is due to a defect of the... -
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- A Case of Kallmann Syndrome Conceived by Administration of Gonadotropin
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Nam YS, Kim NK, Jeong CJ, Cha SH, Cha KY
- KMID: 2262727
- Korean J Obstet Gynecol.
- 2002 Apr;45(4):714-717.
Pulsatile secretion of GnRH from the hypothalamus is a prerequisite for both the initiation and maintenance of the reproductive axis in humans. Failure of this episodic GnRH secretion results in... -
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- A Case of Kallmann's Syndrome with Unilateral Renal Aplasia and Diabetes Mellitus
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Lee EJ, Hong SW, Hong YK, Yoon JS, Mok JO, Kim YJ, Park HK, Kim CH, Kim SJ, Byun DW, Bae WK, Suh KI, Yoo MH
- KMID: 2100459
- J Korean Soc Endocrinol.
- 2005 Feb;20(1):96-102.
- doi: 10.3803/jkes.2005.20.1.96
Kallmann's syndrome is defined as the combination of hypogonadotropic hypogonadism and anosmia/hyposmia. The syndrome is a result of defect in the embryonic migratory pathway of gonadotropin-releasing hormone, which synthesizes neurons... -
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- KAL Gene and GnRH Receptor Gene Analysis in Patients with Kallmann's Syndrome
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Park KH, Mo HJ, Kim JY, Kim JY, Bae SW, Lee BS, Kim IK, Kim SK, Kim KA, Ahn YH
- KMID: 2199559
- J Korean Soc Endocrinol.
- 1999 Dec;14(4):645-656.
BACKGROUND: Kallmann's syndrome is related to the defect in migration of olfactory neuron and GnRH neuron from the olfactory placode to the brain and it represents hypogonadism with anosmia or... -
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- A Case of Kallmann's Syndrome with Frontal Lobe Atrophy and Mental Retardation
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Hyun S, Park S, Kang DG, Jeong SU, Lee DH, Koh G
- KMID: 2169021
- Endocrinol Metab.
- 2010 Jun;25(2):142-146.
- doi: 10.3803/EnM.2010.25.2.142
Kallmann's syndrome is a rare condition, and this is defined as hypogonadotropic hypogonadism and anosmia or hyposmia. The syndrome may be associated with cleft lip, cleft palate, color blindness, skeletal... -
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- A Familial Case of Kallmann Syndrome due to KAL1 Gene Complete Deletion
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Lee SH, Han SW, Kim GH, Yoo HW, Chung WY
- KMID: 1450626
- J Korean Soc Pediatr Endocrinol.
- 2011 Apr;16(1):61-65.
- doi: 10.6065/jkspe.2011.16.1.61
Kallmann syndrome (KS) is characterized by the association of hypogonadotropic hypogonadism and anosmia. Although the vast majority of KS cases are sporadic, some X-linked recessive (KAL1), autosomal dominant (FGFR1), and... -
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- Incidentally Detected Juvenile-Pattern Bone Scintigraphy in a Young Man with Kallmann's Syndrome
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Kwon SH, Chung YS, Lee DH, Jo KS, An YS, Yoon JK, Lee SJ
- KMID: 2313204
- Nucl Med Mol Imaging.
- 2014 Sep;48(3):247-248.
- doi: 10.1007/s13139-014-0264-6
No abstract available. -
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- Genetic Aspects of Idiopathic Hypogonadotropic Hypogonadism
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Shin YL
- KMID: 2192846
- J Korean Soc Pediatr Endocrinol.
- 2010 Dec;15(3):157-163.
Idiopathic hypogonadotropic hypogonadism (IHH) is defined by delayed or absent sexual development associated with inappropriately low gonadal sexual hormone and gonadotropin levels in the absence of anatomical or functional abnormalities... -
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- A Case of Isolated Gonadotropin Deficiency with Negative KALIG-1 Gene
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Nam YS, Lee SH, Kwak IP, Yoon TK, Cha KY
- KMID: 1930526
- Korean J Fertil Steril.
- 1998 Dec;25(3):293-297.
Hypogonadotropic hypogonadism, or the lack of function of the testis or ovary secondary to the lack of pituitary and or hypothalamic trophic hormones, is also sometimes generally termed Kallmann's syndrome.... -
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- Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future
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Kim SH
- KMID: 2169652
- Endocrinol Metab.
- 2015 Dec;30(4):456-466.
- doi: 10.3803/EnM.2015.30.4.456
The proper development and coordination of the hypothalamic-pituitary-gonadal (HPG) axis are essential for normal reproductive competence. The key factor that regulates the function of the HPG axis is gonadotrophin-releasing hormone... -
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- Endocrinologic evaluation of male hypogonadism: Kallmann's syndrome
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Choi HC, Lee IK, Kim CI
- KMID: 1913058
- Korean J Urol.
- 1991 Apr;32(2):311-318.
A clinical investigation and hormonal study was on 36 patients of male hypogonadism who visited the Department of Urology, Dong San hospital, Keimyung university, School of Medicine from March, 1986... -
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