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Case report 848. Kallman's syndrome: hypogonadotropic hypogonadism with delayed closure of epiphyseal growth zones, resulting in epiphysiolysis of the left proximal femoral epiphysis after trauma.

作者信息

Vallier H A, Bergman A G, Kargas S A

机构信息

Department of Radiology, Stanford University Medical Center.

出版信息

Skeletal Radiol. 1994 Jul;23(5):385-7. doi: 10.1007/BF02416999.

DOI:10.1007/BF02416999
PMID:7939840
Abstract
摘要

相似文献

1
Case report 848. Kallman's syndrome: hypogonadotropic hypogonadism with delayed closure of epiphyseal growth zones, resulting in epiphysiolysis of the left proximal femoral epiphysis after trauma.病例报告848. 卡尔曼综合征：促性腺激素缺乏性性腺功能减退伴骨骺生长区闭合延迟，外伤后导致左股骨近端骨骺分离。
Skeletal Radiol. 1994 Jul;23(5):385-7. doi: 10.1007/BF02416999.
2
Slipped capital femoral epiphysis. The mechanical function of the periosteum: new aspects and theory including bilaterality.股骨头骨骺滑脱。骨膜的力学功能：包括双侧性在内的新观点和理论。
Acta Radiol Suppl (Stockholm). 2004 Aug(431):1-27.
3
[Epiphysiolysis of the femur head in hypogonadism of pituitary origin].
Chir Narzadow Ruchu Ortop Pol. 1989;54(1):67-8.
4
Bilateral epiphysiolysis of the femoral heads in two dogs.
J Am Vet Med Assoc. 1997 Apr 15;210(8):1162-5.
5
[Development and functional structure of the epiphyseal plate].[骨骺板的发育与功能结构]
Orthopade. 2002 Sep;31(9):835-40. doi: 10.1007/s00132-002-0359-0.
6
Delayed treatment of a malreduced distant femoral epiphyseal plate fracture.
Med Sci Sports Exerc. 1993 Jun;25(6):761.
7
[Bilateral fractures of the epiphyses of the femur head in a child. A case report].
Aktuelle Traumatol. 1983 Oct;13(5):198-200.
8
Slipped upper femoral epiphysis in a 19-year-old male.
J Pediatr Orthop B. 2010 Jan;19(1):19-21. doi: 10.1097/BPB.0b013e32832efc88.
9
Slipped capital femoral epiphysis: a pathological study. II. An ultrastructural study of 23 cases.股骨头骨骺滑脱：一项病理学研究。II. 23例的超微结构研究
J Pediatr Orthop. 1985 Jan-Feb;5(1):47-58.
10
Physeal dysplasia with slipped capital femoral epiphysis in 13 cats.
Vet Pathol. 2001 Jan;38(1):92-7. doi: 10.1354/vp.38-1-92.

引用本文的文献

1
Panhypopituitarism diagnosed in adulthood: Imaging findings of bone and other organs.成人期诊断的全垂体功能减退症：骨骼及其他器官的影像学表现
Radiol Case Rep. 2023 Jul 29;18(10):3553-3559. doi: 10.1016/j.radcr.2023.07.039. eCollection 2023 Oct.
2
Incidentally Detected Juvenile-Pattern Bone Scintigraphy in a Young Man with Kallmann's Syndrome.一名患有卡尔曼综合征的年轻男性偶然发现的青少年型骨闪烁显像
Nucl Med Mol Imaging. 2014 Sep;48(3):247-8. doi: 10.1007/s13139-014-0264-6. Epub 2014 Feb 15.

本文引用的文献

1
Syndrome of anosmia with hypogonadotropic hypogonadism (Kallmann syndrome): clinical and laboratory studies in 23 cases.嗅觉缺失伴低促性腺激素性性腺功能减退综合征（卡尔曼综合征）：23例临床及实验室研究
Am J Med. 1982 Oct;73(4):506-19. doi: 10.1016/0002-9343(82)90329-1.
2
Isolated gonadotropin deficiency in boys: clinical characteristics and growth.
J Pediatr. 1987 Nov;111(5):684-92. doi: 10.1016/s0022-3476(87)80243-3.
3
Puberty and its disorders in boys.男孩的青春期及其疾病
Endocrinol Metab Clin North Am. 1991 Mar;20(1):43-69.
4
Radiologic manifestations in the musculoskeletal system of miscellaneous endocrine disorders.各种内分泌疾病的肌肉骨骼系统放射学表现。
Radiol Clin North Am. 1991 Jan;29(1):135-47.
5
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.X连锁卡尔曼综合征（促性腺激素缺乏性性腺功能减退症伴嗅觉缺失）定位于Xp22.3：与高变重复序列CRI-S232紧密连锁。
Am J Hum Genet. 1990 Oct;47(4):664-9.
6
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.
Nature. 1991 Oct 10;353(6344):529-36. doi: 10.1038/353529a0.
7
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.X连锁型卡尔曼综合征的候选基因编码一种与黏附分子相关的蛋白质。
Cell. 1991 Oct 18;67(2):423-35. doi: 10.1016/0092-8674(91)90193-3.
8
Pituitary gigantism.垂体性巨人症
Endocrinol Metab Clin North Am. 1992 Sep;21(3):633-47.
9
The effect of pubertal delay on adult height in men with isolated hypogonadotropic hypogonadism.青春期延迟对孤立性促性腺激素缺乏性性腺功能减退男性成年身高的影响。
J Clin Endocrinol Metab. 1992 Feb;74(2):436-40. doi: 10.1210/jcem.74.2.1449545.
10
Familial Kallmann syndrome with unilateral renal aplasia.伴有单侧肾发育不全的家族性卡尔曼综合征。
Clin Genet. 1975 May-Jun;7(5):368-81. doi: 10.1111/j.1399-0004.1975.tb00344.x.