SEVERE INSULIN RESISTANCE AND DIABETES-MELLITUS IN MANDIBULOFACIAL DYSPLASIA

被引:23
作者
FREIDENBERG, GR
CUTLER, DL
JONES, MC
HALL, B
MIER, RJ
CULLER, F
JONES, KL
LOZZIO, C
KAUFMANN, S
机构
[1] UNIV KENTUCKY, DEPT PEDIAT, LOUISVILLE, KY USA
[2] UNIV CALIF SAN DIEGO, DEPT PEDIAT, LA JOLLA, CA 92093 USA
[3] UNIV CALIF SAN DIEGO, DEPT MED, LA JOLLA, CA 92093 USA
[4] UNIV TENNESSEE, DEPT PEDIAT, KNOXVILLE, TN 37996 USA
[5] EMORY UNIV, DEPT PEDIAT, ATLANTA, GA 30322 USA
来源
AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1992年 / 146卷 / 01期
关键词
D O I
10.1001/archpedi.1992.02160130095028
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Mandibuloacral dysplasia (MAD) is a syndrome with onset in midchildhood. The predominant characteristics of MAD include flexion contractures; mandibular hypoplasia; loss of body fat; atrophic, speckled skin; and progressive osteolysis of the clavicles. We studied three males with MAD. Each had lipodystrophy of the extremities, with sparing of the face and neck. All had moderate hyperlipidemia. In response to oral glucose, each had a diabetic response, with peak insulin levels between 2870 and 22 960 pmol/L. Insulin-stimulated glucose disposal was determined in two patients with MAD. At an insulin infusion rate of 120 mU/m2 per minute, glucose disposal was less than 25% of that measured at similar levels of insulinemia in nondiabetic control subjects, indicating marked insulin resistance in patients with MAD. The insulin resistance occurred without obesity, excessive levels of counterregulatory hormones, or anti-insulin-receptor antibodies. We suggest that MAD is a previously undescribed form of lipodystrophic insulin-resistant diabetes mellitus.
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页码:93 / 99
页数:7
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