APLASIA-CUTIS-CONGENITA AND ENLARGED PARIETAL FORAMINA (CATLIN MARKS) IN A FAMILY

被引：15

作者：

PREIS, S ^{[1
]}

ENGELBRECHT, V ^{[1
]}

LENARD, HG ^{[1
]}

机构：

[1] UNIV DUSSELDORF,INST DIAGNOST RADIOL,D-40225 DUSSELDORF,GERMANY

来源：

ACTA PAEDIATRICA | 1995年 / 84卷 / 06期

关键词：

D O I：

10.1111/j.1651-2227.1995.tb13735.x

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

[No abstract available]

引用

页码：701 / 702

页数：2

共 8 条

[1]

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[2]

Singman R, Asaikar S, Hotson G, Prose NS, Aplasia cutis congenita and arteriovenous fistula, Arch Neurol, 47, pp. 1255-1258, (1990)

[3]

McKusick VA, Mendelian inheritance in man, Catalogs of autosomal dominant, autosomal recessive and X‐linked phenotypes, pp. 168-500, (1992)

[4]

Frieden IJ, Aplasia cutis congenita: A clinical review and proposal for classification, J Am Acad Dermatol, 13, pp. 646-660, (1986)

[5]

Goldsmith WM, The Catlin marks: the inheritance of an unusual opening in the parietal bones, J Hered, 13, pp. 69-71, (1922)

[6]

Lother K., Familiäres Vorkommen von Foramina parietalia per‐magna, Arch Kinderheilk, 160, pp. 156-168, (1959)

[7]

Mannino FL, Jones KL, Benirschke K., Congenital skin defects and fetus papyraceus, J Pediatr, 91, pp. 559-564, (1977)

[8]

Hoyme EH, Jones KL, Dixon SD, Jewett T, Hanson JE, Robinson LK, Et al., Prenatal cocaine exposure and fetal vascular disruption, Pediatrics, 85, pp. 743-747, (1990)

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