1) Familial partial lipodystrophy
家族性局部脂肪萎缩
1.
Familial partial lipodystrophy (FPLD) is autosomal dominant inheritance, and generally characterized by progressive and gradual subcutaneous adipose tissue loss from the extremities, classically commencing in puberty, accompanied by variable adipose tissue loss in the trunk and chest, prominent, well-defined musculature, together with excess fat deposi- tion within the face, neck and visceral fat.
按不同的遗传规律和临床表现可分为遗传性全身脂肪萎缩(CGL)、家族性局部脂肪萎缩(FPLD)、获得性局部脂肪萎缩(APL)、获得性全身脂肪萎缩(AGL)。
2) localized lipoatrophy
局限性脂肪萎缩
3) lipoatrophic
脂肪萎缩的
4) lipoatrophic diabetes
脂肪萎缩性糖尿病
1.
Some specific types of diabetes, such as MODY, Leprechaunism, lipoatrophic diabetes, and Rabson-Mendenhall syndrome, are monogenic forms of diabetes and are inherited as a Mendelian pattern.
一些特殊类型的糖尿病,如:青年发病的成年型糖尿病、矮妖精貌综合征、脂肪萎缩性糖尿病和Rabson-Mendenhall综合征为单基因致病并符合孟德尔遗传。
5) familial progressive spinal muscular atrophy
家族性进行性脊肌萎缩
6) familial amyotrophic lateral sclerosis
家族性肌萎缩侧索硬化
补充资料：家族性
家族性
familial
在家族中一再出现的性状或疾病。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条