1) lipoatrophic
脂肪萎缩的
2) localized lipoatrophy
局限性脂肪萎缩
3) lipoatrophy
皮下脂肪萎缩
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 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)。
6) Diminishable core
萎缩的核
补充资料：局限性骨化性肌炎
局限性骨化性肌炎
local myositis ossificans
多见于肌肉直接损伤后，如股四头肌、肱肌、髋内收肌等，血肿机化，成纤维细胞增殖，骨样组织形成，并分泌碱性磷酸酶。伤后6～8周出现骨化。关键在于预防。在骨折或关节脱位进行复位过程中，操作必须轻柔，以减少肌肉或韧带的损伤。禁止在没有麻醉情况下进行粗暴的反复操作。
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