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Hereditary hypotrichosis. A previously undescribed syndrome.

作者信息

Bentley-Phillips B, Grace H J

出版信息

Br J Dermatol. 1979 Sep;101(3):331-9.

PMID:508598
Abstract

A syndrome of hereditary hypotrichosis with an unusual natural history and clinical features was encountered in a Caucasian family of four generations with a total of twenty-four members of whom eleven were affected. The mode of inheritance was autosomal dominant with variable penetrance. The loss of hair involved the scalp, eyebrows, eyelashes and body hair, manifesting itself in the school years and progressing to almost complete baldness. There were no associated abnormalities and no sex limitation. Clinical, genetic, biochemical, mechanical, histological and immunological aspects were studied. Essential differences between this type of hereditary hypotrichosis and others previously recorded are stressed.

摘要

相似文献

1
Hereditary hypotrichosis. A previously undescribed syndrome.
Br J Dermatol. 1979 Sep;101(3):331-9.
2
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An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family.在一个意大利家族中,一种常染色体显性遗传的单纯遗传性少毛症被定位到18号染色体短臂11.32 - 11.23区域。
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[Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy].
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引用本文的文献

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A Novel Pathogenic CDH3 Variant underlying Heredity Hypotrichosis Simplex detected by Whole-Exome Sequencing (WES)-A Case Report.通过全外显子组测序(WES)检测到的一种导致单纯遗传性少毛症的新型致病CDH3变异——病例报告
Cold Spring Harb Mol Case Stud. 2022 Aug 5;8(5). doi: 10.1101/mcs.a006225.
2
Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family.常染色体隐性单纯性少毛症伴羊毛状发:一个新家族的报告
Dermatol Reports. 2011 Aug 3;3(2):e13. doi: 10.4081/dr.2011.e13.
3
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.玛丽·乌纳少毛症基因定位于D8S258和D8S298之间:通过cDNA和基因组测序排除hr基因。
Am J Hum Genet. 1999 Aug;65(2):413-9. doi: 10.1086/302506.