عنوان المقالة: Pulmonary Alveolar microlithiasis.Report of two brothers with the same illness and review of literature
الاستاذ الدكتور حسين آل سردار | Hussain.Al Sardar | 4102
- نوع النشر
- مجلة علمية
- المؤلفون بالعربي
- المؤلفون بالإنجليزي
- Hussain Al-Sardar 1, Dhaher J S Al-Habbo, Rami M A Al-Hayali
- الملخص الانجليزي
- Pulmonary alveolar microlithiasis (PAM) is a rare lung disease characterised by extensive deposition of calpospherites within the alveoli. The disease is caused by mutations in the gene SLC34A2 encoding sodium-dependent phosphate co-transporter. It is an autosomal recessive disease with sporadic cases worldwide. Most patients are asymptomatic at the time of diagnosis. It may progress slowly over years to respiratory failure and cor pulmonale.
- تاريخ النشر
- 31/03/2014
- الناشر
- Hussain Al-Sardar 1, Dhaher J S Al-Habbo, Rami M A Al-Hayali
- رقم المجلد
- رقم العدد
- رابط DOI
- 10.1136/bcr-2013-201300
- الصفحات
- 2
- الكلمات المفتاحية
- Pulmonary,microlithiasis,alvolar