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- W2393439790 abstract "Objective To analyse the clinical characteristics of 221 microsomia children whose mean stature is lower than that of the same age and same sex 2SD or who is under the third percentage.Methods Uniform investigation was adopted for diseased history,physical examination,all kinds of laboratory tests and treatment.Results Among the 221 cases of the microsomia children,75 of them(36.6%) were growth hormone deficiency.Among the 75 cases of GHD,57 of them(76%) had abnormal birth.The treatmental effectiveness by rhGH was obviously;The number of constitutional growth delay children was 43 cases(19.5%),the number of familiar short stature children was 42 cases(19%),Among them,63 cases(74%)had family history;Among 221 microsomia children,2l of them(9.5%)were congenital hypothyroidism.The treatment with the substitution of thyroxine had a good result.Conclusion The growth hormone deficiency,constitutional growth delay and familiar short stature are the common types in the microsomia children.The measure to improve the situation is to qualify the circumnatal period,perform the pre-natal check-up." @default.
- W2393439790 created "2016-06-24" @default.
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- W2393439790 date "2006-01-01" @default.
- W2393439790 modified "2023-09-25" @default.
- W2393439790 title "Clinical Analysis of Microsomia Children" @default.
- W2393439790 hasPublicationYear "2006" @default.
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