BMJ Best Practice
最后审核时间: 六月 2019
最近更新时间: 三月 2019

小结

鉴别诊断

常见

  • 家族性身材矮小症(遗传性身材矮小症)
  • 生长发育全面滞后 (CDGD)
  • 特发性身材矮小
  • 小于胎龄儿(SGA)至2岁时无追赶性生长

罕见

  •  生长激素(GH)缺乏
  •  甲状腺功能减退
  •  库欣综合征
  • 生长激素不敏感(Laron侏儒症)

贡献者

Renee Bargman MS, MD

Director of Pediatric Endocrinology

Nassau University Medical Center

East Meadow

NY

利益冲突披露
RB declares that she has no competing interests.
Maria Vogiatzi MD

Associate Professor of Pediatrics - Clinician Educator

Division of Endocrinology and Diabetes

Children's Hospital of Philadelphia

Philadelphia

PA

利益冲突披露
MV declares that she has no competing interests.

同行评议专家 查看所有

Chief of the Division of Pediatric Endocrinology

Assistant Professor

UMDNJ-Robert Wood Johnson Medical School

New Brunswick

NY

利益冲突披露
IM declares that he has no competing interests.

Professor of Pediatrics

Director

Pediatric Endocrinology

New York University Medical Center

New York

NY

利益冲突披露
RD declares that he has no competing interests.

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