|
��չ����
|
|
| ������Ϣ | |
 |
Supporting info |
|
PDFȫ�� |
|
[HTMLȫ��] |
|
����� |
| �����뷴�� | |
|
�������ù����� |
|
���� |
|
Email Alert |
|
���·��� |
|
���������Ϣ |
| ���Ĺؼ���������� | |
|
ɫ�س����쳣 |
|
�Ŵ� |
| ��������������� | |
|
���� |
|
�� |
| PubMed | |
|
Article by Xiong,y |
|
Article by Ci,b |
�Ŵ��Է�����ɫ���쳣֢
����1,��2
1. �Ϸ�ҽ�ƴ�ѧ���������и��ױ���Ժ
2. �����е�������ҽԺ
�Ŵ��Է�����ɫ���쳣֢��һ���ټ��ij�Ⱦɫ�������Ŵ���Ƥ������Ƥ����Ҫ����Ϊȫ������ɫ�س��Űߺ�ɫ�ؼ��˰ߡ��ò��÷����������������о���Ϊ���Ŵ��ԶԳ���ɫ���쳣֢�Ǹò���һ�����͡��������Ŷ��²�����������о��������Ŵ��ԶԳ���ɫ���쳣֢���Ŵ��Է�����ɫ���쳣֢�����ͬ�ļ�����
Dyschromatosis universalis hereditaria
Dyschromatosis universalis hereditaria is a rare autosomal dominant inherited disease characterized by generalized hyper- and hypo-pigmentation of the skin. Most of the reported cases of this disease are from east Asian. Early studies suggested that dyschromatosis symmetrica hereditaria might be a subtype of this disease. However, recent studies on pathogenic genes have revealed that dyschromatosis symmetrica hereditaria and dyschromatosis universalis hereditaria belong to two distinct disease entities.
�����пƼ��� ��200803141;�м�����