Literature DB >> 7636061

Shwachman-Diamond syndrome associated with hypogammaglobulinemia and growth hormone deficiency.

S J Kornfeld1, J Kratz, F Diamond, N K Day, R A Good.   

Abstract

Shwachman-Diamond syndrome is a rare congenital disorder of unknown etiology. Characteristic abnormalities of this disease include pancreatic insufficiency, skeletal anomalies, growth retardation, recurrent infections, and hematologic abnormalities. Significant morbidity and mortality in these patients result from respiratory infections, which are not well explained on the basis of neutrophil defects. We have had the opportunity to perform an in-depth clinical immunologic and endocrinologic evaluation of a patient with this syndrome with recurrent respiratory tract infections. She was found to have profound humoral immunologic defects, and serum thymulin was absent. In addition, endocrinologic evaluation for growth retardation revealed growth hormone deficiency. The patient responded to treatment with supplemental growth hormone and intravenous gammaglobulin with accelerated growth and cessation of infections. This case is unique in that it links growth hormone deficiency and hypogammaglobulinemia in a non-X-linked manner and may provide the basis for treatment of other patients with this rare syndrome.

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Year:  1995        PMID: 7636061     DOI: 10.1016/s0091-6749(95)70014-5

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  7 in total

1.  X-linked lymphoproliferative disease associated with hypogammaglobulinemia and growth-hormone deficiency.

Authors:  Abdullah Alangari; Abdullah Abobaker; Hirokazu Kanegane; Toshio Miyawaki
Journal:  Eur J Pediatr       Date:  2005-11-17       Impact factor: 3.183

2.  Endocrine evaluation of children with and without Shwachman-Bodian-Diamond syndrome gene mutations and Shwachman-Diamond syndrome.

Authors:  Kasiani C Myers; Susan R Rose; Meilan M Rutter; Parinda A Mehta; Jane C Khoury; Theresa Cole; Richard E Harris
Journal:  J Pediatr       Date:  2013-01-08       Impact factor: 4.406

Review 3.  Shwachman-Diamond syndrome.

Authors:  C Dall'oca; M Bondi; M Merlini; M Cipolli; F Lavini; P Bartolozzi
Journal:  Musculoskelet Surg       Date:  2011-12-27

4.  Clinical and genetic analyses of presumed Shwachman-Diamond syndrome in Japan.

Authors:  Hiromichi Taneichi; Hirokazu Kanegane; Takeshi Futatani; Keisuke Otsubo; Keiko Nomura; Yuya Sato; Asahito Hama; Seiji Kojima; Urara Kohdera; Takahide Nakano; Hiroki Hori; Hisashi Kawashima; Yoko Inoh; Junji Kamizono; Naoto Adachi; Yuko Osugi; Haruo Mizuno; Noriko Hotta; Hiroshi Yoneyama; Eiji Nakashima; Shiro Ikegawa; Toshio Miyawaki
Journal:  Int J Hematol       Date:  2006-07       Impact factor: 2.490

Review 5.  Shwachman-Diamond syndrome: a review of the clinical presentation, molecular pathogenesis, diagnosis, and treatment.

Authors:  Lauri Burroughs; Ann Woolfrey; Akiko Shimamura
Journal:  Hematol Oncol Clin North Am       Date:  2009-04       Impact factor: 3.722

Review 6.  Some cases of common variable immunodeficiency may be due to a mutation in the SBDS gene of Shwachman-Diamond syndrome.

Authors:  S Khan; J Hinks; J Shorto; M J Schwarz; W A C Sewell
Journal:  Clin Exp Immunol       Date:  2008-01-10       Impact factor: 4.330

7.  A pediatric genetic disorder diagnosed in adulthood.

Authors:  Joseph A Church
Journal:  PLoS Med       Date:  2006-01-31       Impact factor: 11.069

  7 in total

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