Abstract | OBJECTIVE: DESIGN AND METHODS: Case series with germline screening of AIP and haplotype analyses among R271W families. RESULTS: This previously unreported kindred consisted of three affected individuals that either presented with or had first symptoms of a pituitary macroadenoma in late childhood or adolescence. The index case, a 15-year-old male with incipient gigantism and his maternal aunt, had somatotropinomas, and the maternal uncle of the index case had a prolactinoma. All tumors were large (15, 40, and 60 mm maximum diameter) and two required transcranial surgery and radiotherapy. All three affected subjects and ten other unaffected relatives were found to be positive for a germline R271W AIP mutation. Comparison of the single nucleotide polymorphism patterns among this family and two previously reported European FIPA families with the same R271W mutation demonstrated no common ancestry. CONCLUSIONS: This kindred exemplifies the aggressive features of pituitary adenomas associated with AIP mutations, while genetic analyses among three R271W FIPA families indicate that R271W represents a mutational hotspot that should be studied further in functional studies.
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Authors | Juliet E Jennings, Marianthi Georgitsi, Ian Holdaway, Adrian F Daly, Maria Tichomirowa, Albert Beckers, Lauri A Aaltonen, Auli Karhu, Fergus J Cameron |
Journal | European journal of endocrinology
(Eur J Endocrinol)
Vol. 161
Issue 5
Pg. 799-804
(Nov 2009)
ISSN: 1479-683X [Electronic] England |
PMID | 19684062
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Intracellular Signaling Peptides and Proteins
- aryl hydrocarbon receptor-interacting protein
- DNA
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Topics |
- Adenoma
(genetics)
- Adolescent
- Adult
- Australia
- DNA
(chemistry, genetics)
- Female
- Genetic Variation
- Germ-Line Mutation
- Humans
- Intracellular Signaling Peptides and Proteins
(genetics)
- Male
- New Zealand
- Pedigree
- Pituitary Neoplasms
(genetics)
- Point Mutation
- Polynesia
(ethnology)
- Sequence Analysis, DNA
- Young Adult
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