Skin markers of X-linked dominant chondrodysplasia punctata

1979 ◽  
Vol 115 (8) ◽  
pp. 931b-932 ◽  
Author(s):  
R. Happle
2013 ◽  
Vol 17 ◽  
pp. S14
Author(s):  
AM Bams-Mengerink ◽  
JHTM Koelman ◽  
H Waterham ◽  
PG Barth ◽  
BT Poll-The

2017 ◽  
Vol 7 (1) ◽  
pp. e16
Author(s):  
Yuki Tanaka ◽  
Kei Watanabe ◽  
Keiichi Katsumi ◽  
Masayuki Ohashi ◽  
Keisuke Nagasaki ◽  
...  

1993 ◽  
Vol 45 (1) ◽  
pp. 101-104 ◽  
Author(s):  
Tsutomu Ogata ◽  
Peter Goodfellow ◽  
Christine Petit ◽  
Pierre Maroteaux ◽  
Nobutake Matsuo

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shuzo Kato ◽  
Nobuyuki Fujita ◽  
Satoshi Suzuki ◽  
Osahiko Tsuji ◽  
Narihito Nagoshi ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Nalan Karabayır ◽  
Gonca Keskindemirci ◽  
Erdal Adal ◽  
Orhan Korkmaz

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.


2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Guannan He ◽  
Yan Yin ◽  
Jing Zhao ◽  
Xueyan Wang ◽  
Jiaxiang Yang ◽  
...  

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