A NOVEL MUTATION INVOLVING AN INSERTION IN EXON 4 OF THE APC GENE LEADING TO AN UNCOMMON PHENOTYPE

2004 ◽  
Vol 99 ◽  
pp. S113
Author(s):  
Ethan D. Miller ◽  
Howard Hampel ◽  
Richard W. Goodgame
Keyword(s):  
Apc Gene ◽  
2003 ◽  
Vol 123A (2) ◽  
pp. 169-171 ◽  
Author(s):  
Bozena Marszalek ◽  
Slawomir A. Wisniewski ◽  
Piotr Wojcicki ◽  
Kazimierz Kobus ◽  
Wieslaw H. Trzeciak

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 5140-5140
Author(s):  
Rong-Fu Zhou ◽  
Hong Tao ◽  
Jian Ouyang ◽  
Xian Zhang ◽  
Yonggong Yang ◽  
...  

Abstract Abstract 5140 Objective To identify gene mutations for one patient and his family members with protein S and antithrombin deficiency. Methods ELISA were used to detect protein S (PS), protein C (PC) and antithrombin (AT) activities for the proband and family members, respectively. The genomic DNA was extracted from the peripheral blood of proband and family members. All exons and their flanks of protein S gene and antithrombin gene were amplified by polymerase chain reaction (PCR). The PCR products were sequenced directly. The mutation-related exons of his famliy members were amplified by PCR and sequenced directly. Results The proband was a 49-year-old male. He presented with sudden left lower extremity swelling and pain without casues. Regular examination revealed that his APTT, PT, and TT were all in normal levels, but D- dimmer was 5. 62mg/L, Color doppler ultrasonography showed thrombosis in his left femoral vein. The activity of PS for his family members was ‡1 0%, ‡2 0%, ‡3 0%, ‡4 130. 8%, ‡5 8. 4%, ‡1 0%, ‡2 0%, and that of AT was ‡1 129. 1%, ‡2 51. 9%, ‡3 73.2%, ‡4 119. 1%, ‡5 136. 2%, ‡1 65. 5% and ‡2 60. 1%, respectively. The sequencing analysis showed that a heterozygous missense mutation G68395T (NG_009813. 1) was detected in Exon 4 of PS gene leading to the substitution of Arg90 by Leu (NP_000304. 2) for the propositus. The heterozygous mutation (Arg90Leu) was also found in other family members. A heterozygous (nonsense) mutation G12444A (NG_012462. 1) was detected in Exon 4 of AT gene leading to Trp257Ter (NP_000479. 1) for the propositus. The mutation (Trp257Ter) was found in other family members with reduced activity of AT. These two mutations (G68395T in PS gene and G12444A in AT gene) were not reported before and were thus novel ones. Conclusion The novel mutation G68395T in PS gene and G12444A in AT gene might be the causes of deficiency of PS and AT for the family. Disclosures: No relevant conflicts of interest to declare.


2017 ◽  
Vol 22 (1) ◽  
pp. 152-162 ◽  
Author(s):  
Fang Yu ◽  
Wenping Cai ◽  
Beizhan Jiang ◽  
Laijun Xu ◽  
Shangfeng Liu ◽  
...  

1997 ◽  
Vol 10 (1) ◽  
pp. 86-87 ◽  
Author(s):  
Laurent Gouya ◽  
Olivier Pascaud ◽  
Anne Munck ◽  
Jacques Elion ◽  
Erick Denamur
Keyword(s):  

1994 ◽  
Vol 3 (3) ◽  
pp. 305-308 ◽  
Author(s):  
Alessandro Cama ◽  
Diana L. Esposito ◽  
Raffaele Palmirotta ◽  
Maria Cristina Curia ◽  
Annalisa Ranieri ◽  
...  

2016 ◽  
Vol 124 (7) ◽  
pp. 485-492 ◽  
Author(s):  
Derek B. Allison ◽  
Mohammed T. Lilo ◽  
Susan Geddes ◽  
Aparna Pallavajjalla ◽  
Frederic Askin ◽  
...  

2021 ◽  
Author(s):  
Xiao-Hui Tao ◽  
Xing-Guang Yang ◽  
Zi-Yuan Wang ◽  
Yang Xu ◽  
Zhen-Lin Zhang ◽  
...  

Abstract BackgroundTo investigate the clinical characteristics and molecular diagnosis of progressive diaphyseal dysplasia (PDD) in three unrelated Chinese families. MethodsThe present study recruited six patients aged 14 to 45 from three unrelated families with PDD, including five females and one male. Clinical manifestations, biochemical tests, radiographic examinations were analyzed and the TGF-β1 gene mutation was further identified by Sanger sequencing. In addition, data of treatment and follow-up were also collected.ResultsThe onset age of the patients ranged from 1 to 6 years. All the affected patients had family histories and were consisted with autosomal dominant inheritance pattern. All of them exhibited gait disturbance, fatigue, progressive bone pain, as well as muscle atrophy and weakness in limbs. Notably, there was one 15-year-old girl who experienced heart valve defects and tachycardia at birth. Laboratory examinations revealed the inflammatory markers were in high level, besides the extremely increased bone metabolism indicators. The thickened diaphysis of long bones and the narrowed medullary cavity were observed by radiography. Furthermore, radionuclide bone scan detected abnormal symmetrical radioactive concentration in the affected regions of bone. Sanger sequencing identified a missense heterozygous mutation in exon 4 of TGF-β1 gene, resulting in R218C, which confirmed PDD eventually. More important, a novel mutation c.669C>G in exon 4 of TGF-β1 gene harboring C223W were detected in family 3. Subsequent bioinformatics software predicted that the novel mutation was pathogenic. Our study also showed that zoledronic acid was not effective in the control of bone turnover markers and the relief of bone pain in patients with PDD.ConclusionIn addition to the typical PDD manifestations, the new phenotypic characteristics such as tachycardia and heart valve defect were firstly reported in one female patient carried the novel mutation p.Cys223Trp in TGF-β1 gene. In addition, our study indicated that the increased bone metabolism indicators and inflammatory markers may possess auxiliary diagnosis for PDD. More importantly, zoledronic acid was used to treat PDD patients in this study. After one-year follow-up, it was proved that the drug effect was not satisfactory, and new drugs need to be developed to treat the disease.


2011 ◽  
Vol 6 (6) ◽  
pp. 627-635 ◽  
Author(s):  
Wang Qiong ◽  
Fang Chao ◽  
Liu Wu-Jun ◽  
Fang Yi ◽  
Yu Shi-Gang

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