Congenital absence of pituitary gland and adrenal hypoplasia.
作者信息
Moncrieff M W, Hill D S, Archer J, Arthur L J
出版信息
Arch Dis Child. 1972 Feb;47(251):136-7. doi: 10.1136/adc.47.251.136.
Abstract
摘要
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1
Congenital absence of pituitary gland and adrenal hypoplasia.先天性垂体缺如和肾上腺发育不全。
Arch Dis Child. 1972 Feb;47(251):136-7. doi: 10.1136/adc.47.251.136.
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[Congenital secondary adrenal hypoplasia with hypoglycemia (author's transl)].
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Idiopathic adrenal hypoplasia in children.儿童特发性肾上腺发育不全
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[Cytology of the anterior pituitary in adrenocortical hypoplasia with hypoglycaemia].[肾上腺皮质发育不全伴低血糖时垂体前叶的细胞学]
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[Familial congenital adrenal hypoplasia with failure of the adrenal cortex].[家族性先天性肾上腺发育不全伴肾上腺皮质功能衰竭]
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Hypoplasia of the anterior pituitary and neonatal hypoglycemia.
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Anterior pituitary and adrenal absence in a live-born normocephalic infant.
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Coal-black hyperpigmentation at birth in a child with congenital adrenal hypoplasia.一名患有先天性肾上腺发育不全的儿童出生时出现煤黑色色素沉着。
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引用本文的文献
1
Micropenis: an important early sign of congenital hypopituitarism.小阴茎：先天性垂体功能减退的重要早期体征。
Br Med J (Clin Res Ed). 1984 Feb 25;288(6417):621-2. doi: 10.1136/bmj.288.6417.621.
2
Familial syndrome with panhypopituitarism, hypoplasia of the hypophysis, and poorly developed sella turcica.伴有全垂体功能减退、垂体发育不全及蝶鞍发育不良的家族性综合征。
Arch Dis Child. 1978 Aug;53(8):664-7. doi: 10.1136/adc.53.8.664.
本文引用的文献
1
Congenital absence of the pituitary gland.垂体先天性缺失。
J Pediatr. 1960 May;56:658-64. doi: 10.1016/s0022-3476(60)80341-1.
2
FOUR CLINICAL VARIANTS OF CONGENITAL ADRENAL HYPERPLASIA.先天性肾上腺皮质增生症的四种临床变体
Arch Dis Child. 1964 Feb;39(203):66-72. doi: 10.1136/adc.39.203.66.
3
Hypopituitarism, hypoadrenalism, and hypogonadism in the newborn infant.
J Pediatr. 1956 Jun;48(6):782-92. doi: 10.1016/s0022-3476(56)80210-2.
4
Hypoplasia of the pituitary and adrenal cortex; report of occurrence in twin siblings and autopsy findings.
J Pediatr. 1956 May;48(5):633-9. doi: 10.1016/s0022-3476(56)80097-8.
5
Anterior pituitary and adrenal absence in a live-born normocephalic infant.
Am J Obstet Gynecol. 1966 Nov 15;96(6):893-4. doi: 10.1016/0002-9378(66)90688-0.
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