[ English | Bahasa Malaysia ] Hari ini ialah 25 Mar 2023, 01:29 PM (Terakhir dikemaskini pada: 24th Mar 2023)

Text Red Text Black Text Blue Text Green Text Smaller Text Reset Text Larger

Publication Details
Year :


Journal :

Chai Teng Chear, Harvindar Kaur Gill, Nazatul Haslina Ramly, Jasbir Singh Dhaliwal, Noraini Bujang, Adiratna Mat Ripen and Saharuddin Bin Mohamad (2013). A novel Bruton's Tyrosine Kinase Gene (BTK) invariant splice site mutation in a Malaysian Family with X-Linked Agammaglobulinemia. Asian Pacific Journal Allergy and Immunology 31(4): 320-324

Abstract :

X-linked agammaglobulinemia (XLA) is a rare genetic disorder caused by mutations in the Bruton's tyrosine kinase (BTK) gene. These mutations cause defects in early B cell development. A patient with no circulating B cells and low serum immunoglobulin isotypes was studied as were his mother and sister. Monocyte BTK protein expression was evaluated by flow cytometry. The mutation was determined using PCR and followed by sequencing. Flow cytometry showed the patient lacked BTK protein expression in his monocytes while the mother and sister had 62% and 40% of the monocytes showing BTK protein expressions respectively. The patient had a novel base substitution in the first nucleotide of intron 9 in the BTK gene, and the mutation was IVS9+1G>C. This mutation resulted in exon 9 skipping. This defect rendered the patient susceptible to asthma, failure to thrive, recurrent pyogenic infections, otitis media and bronchopneumonia. His mother and sister were heterozygous for this mutation. The combination of flow cytometry and genetic study is necessary in the diagnosis of X-linked agammaglobulinemia and may be used for subsequent genetic counseling, carrier detection and prenatal diagnosis.




Laman ini sesuai dilihat menggunakan Firefox (24.0) dengan resolusi 1280 x 768 pixels atau lebih.

Lokasi Kami


Kami terletak di Jalan Pahang, 50588 Kuala Lumpur, Malaysia. Klik pada imej peta untuk melancarkan servis Google Maps.

Hubungi Kami