Literature DB >> 10404460

Multiple neonatal endocrinopathies in McCune-Albright syndrome.

P Bareille1, C Azcona, R Stanhope.   

Abstract

Two cases of McCune-Albright syndrome (MAS) are reported who presented in the neonatal period with profound failure to thrive, cardio-respiratory distress, precocious puberty and Cushing's syndrome for which both underwent bilateral adrenalectomy. Both girls had also bilateral nephrocalcinosis; in one case that may have been attributed to Cushing's syndrome, but in the second case the cause remained obscure with no obvious abnormality of calcium metabolism. The first girl had hydrocephalus which is uncommon in this condition and the second girl still failed to thrive at the age of 6 years, despite adequate caloric intake and hormonal manipulation. A constellation of other abnormal features are described. These cases illustrate the complexity of MAS which can become a life-threatening or a debilitating disorder.

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Year:  1999        PMID: 10404460     DOI: 10.1046/j.1440-1754.1999.00337.x

Source DB:  PubMed          Journal:  J Paediatr Child Health        ISSN: 1034-4810            Impact factor:   1.954


  3 in total

1.  A novel, complex heterozygous mutation within Gsalpha gene in patient with McCune-Albright syndrome.

Authors:  Huai-Dong Song; Feng-Ling Chen; Wen-Jing Shi; Shu Wang; Qun Zhang; Ren-Ming Hu; Jia-Lun Chen
Journal:  Endocrine       Date:  2002-07       Impact factor: 3.633

2.  Cushing syndrome in the McCune-Albright syndrome.

Authors:  Rebecca J Brown; Marilyn H Kelly; Michael T Collins
Journal:  J Clin Endocrinol Metab       Date:  2010-02-15       Impact factor: 5.958

3.  Neonatal McCune-Albright Syndrome: A Unique Syndromic Profile With an Unfavorable Outcome.

Authors:  Alessandro Corsi; Natasha Cherman; David L Donaldson; Pamela G Robey; Michael T Collins; Mara Riminucci
Journal:  JBMR Plus       Date:  2019-01-15
  3 in total

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