A Case of Rhizomelic Chondrodysplasia Punctata in Newborn

المؤلفون المشاركون

Korkmaz, Orhan
Karabayır, Nalan
Adal, Erdal
Keskindemirci, Gonca

المصدر

Case Reports in Medicine

العدد

المجلد 2014، العدد 2014 (31 ديسمبر/كانون الأول 2014)، ص ص. 1-3، 3ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2014-03-09

دولة النشر

مصر

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الملخص EN

Rhizomelic chondrodysplasia punctate (RCDP) is a rare autosomal recessive peroxisomal disease.

The main features of the disease are shortening of the proximal long bones, punctate calcifications located in the epiphyses of long bones and in soft tissues around joints and vertebral column, vertebral clefting, dysmorphic face, and severe growth retardation, whereas cervical spinal stenosis may also rarely be present.

Imaging of the brain and spinal cord in patients with this disorder may aid prognosis and guide management decisions.

We report the newborn diagnosed as CDP with cervical stenosis.

Our aim is to discuss current knowledge on etiopathogenesis as well as radiological and clinical symptoms of diseases associated with CDP.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Karabayır, Nalan& Keskindemirci, Gonca& Adal, Erdal& Korkmaz, Orhan. 2014. A Case of Rhizomelic Chondrodysplasia Punctata in Newborn. Case Reports in Medicine،Vol. 2014, no. 2014, pp.1-3.
https://search.emarefa.net/detail/BIM-505666

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Karabayır, Nalan…[et al.]. A Case of Rhizomelic Chondrodysplasia Punctata in Newborn. Case Reports in Medicine No. 2014 (2014), pp.1-3.
https://search.emarefa.net/detail/BIM-505666

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Karabayır, Nalan& Keskindemirci, Gonca& Adal, Erdal& Korkmaz, Orhan. A Case of Rhizomelic Chondrodysplasia Punctata in Newborn. Case Reports in Medicine. 2014. Vol. 2014, no. 2014, pp.1-3.
https://search.emarefa.net/detail/BIM-505666

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-505666