MULTIPLE PITUITARY-HORMONE DEFICIENCIES IN 8 SIBLINGS OF ONE JEWISH MOROCCAN FAMILY

被引：13

作者：

ADLERBIER, M

PERTZELAN, A

LARON, Z

LIEBERMAN, E

MOSES, S

机构：

[1] BEILINSON MED CTR, INST PEDIAT & ADOLESCENT ENDOCRINOL, Petah Tiqwa, ISRAEL

[2] TEL AVIV UNIV, SACKLER SCH MED, RAMAT AVIV, ISRAEL

[3] BEN GURION UNIV NEGEV, FAC HLTH SCI, SOROKA MED CTR, DIV PEDIAT, BEER SHEVA 84120, ISRAEL

来源：

ACTA PAEDIATRICA SCANDINAVICA | 1979年 / 68卷 / 03期

关键词：

genetic markers; panhypopituitarism; Pituitary hormones;

D O I：

10.1111/j.1651-2227.1979.tb05027.x

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Abstract. In a Jewish Moroccan inbred family, 8 of 12 siblings were found to have multiple deficiencies of pituitary hormones, including GH, TSH and gonadotrophins. The parents showed no deficiency and are in good health, as are the other 4 siblings. The investigations carried out indicate that in this family the etiology is hereditary in nature, probably being autosomal recessive, with the defect located in the pituitary gland. Copyright © 1979, Wiley Blackwell. All rights reserved

引用

页码：401 / 404

页数：4

共 16 条

[1]

ADAM A, UNPUBLISHED

[2] HYPOPITUITARISM, HYPOADRENALISM, AND HYPOGONADISM IN THE NEWBORN INFANT [J].