Hereditary 1,25-dihydroxyvitamin D-resistant rickets : a report of several cases in a kindred
المؤلفون المشاركون
al-Arid, Shaykhah Salim
Khan, I. Mannan
al-Abbasi, A. Jabbar
al-Rufai, Muhammad
al-Hirmi, Badriyah
المصدر
العدد
المجلد 18، العدد 1 (31 مارس/آذار 1996)3ص.
الناشر
تاريخ النشر
1996-03-31
دولة النشر
البحرين
عدد الصفحات
3
التخصصات الرئيسية
الملخص EN
We report a Bahraini family with five cases of vitamin D resistant rickets and alopecia.
Investigation confirmed the diagnosis of hereditary vitamin D resistant rickets, type II in 2 of the siblings who were fully investigated.
Although we do not have data to support it, we believe all the sibs had the same type of rickets.
Bahrain Med Bull 1996;18(1): Hereditary 1,25-dihydroxyvitamin D resistant rickets (HVDRR), also known as vitamin D-dependent type II rickets, is a rare autosomal recessive disorder1 .
It results from defective response of the target tissues to the active hormonal form of vitamin D [1,25 (OH)2,D3].
The syndrome is characterised clinically by early onset of rickets with hypocalcemia, hypophosphatemia, secondary hyperparathyroidism in the presence of normal or elevated circulating levels of 1,25 (OH)2 D32,3.
Affected patients in half the kindred's show either partial or total alopecia.
The unresponsiveness of the target tissues to 1,25(OH)2 D3 has been proven to result from mutations in the gene encoding the vitamin D receptor (VDR).
These mutations adversely affect the structure and function of VDR for calcitriol.
In this paper we report our findings in 5 siblings from a Bahraini family of consanguineous marriage who presented to us with vitamin D-resistant rickets and alopecia.
The clinical picture and the course of the disease were similar in all the siblings.
However, since not all these sibs were investigated we have chosen to present the clinical profile of only 2 siblings who were investigated in details.
To the best of our knowledge this is the first case of HVDRR from the Arabian Gulf region.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Khan, I. Mannan& al-Hirmi, Badriyah& al-Abbasi, A. Jabbar& al-Rufai, Muhammad& al-Arid, Shaykhah Salim. 1996. Hereditary 1,25-dihydroxyvitamin D-resistant rickets : a report of several cases in a kindred. Bahrain Medical Bulletin،Vol. 18, no. 1.
https://search.emarefa.net/detail/BIM-605791
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Khan, I. Mannan…[et al.]. Hereditary 1,25-dihydroxyvitamin D-resistant rickets : a report of several cases in a kindred. Bahrain Medical Bulletin Vol. 18, no. 1 (Mar. 1996).
https://search.emarefa.net/detail/BIM-605791
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Khan, I. Mannan& al-Hirmi, Badriyah& al-Abbasi, A. Jabbar& al-Rufai, Muhammad& al-Arid, Shaykhah Salim. Hereditary 1,25-dihydroxyvitamin D-resistant rickets : a report of several cases in a kindred. Bahrain Medical Bulletin. 1996. Vol. 18, no. 1.
https://search.emarefa.net/detail/BIM-605791
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references
رقم السجل
BIM-605791
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
تقوم هذه الخدمة بالتحقق من التشابه أو الانتحال في الأبحاث والمقالات العلمية والأطروحات الجامعية والكتب والأبحاث باللغة العربية، وتحديد درجة التشابه أو أصالة الأعمال البحثية وحماية ملكيتها الفكرية. تعرف اكثر