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[Ichthyosis vulgaris, growth retardation, hair dysplasia, tooth abnormalities, immunologic deficiencies, psychomotor retardation and resorption disorders. Case report of 2 siblings].

作者信息

Braun-Falco O, Ring J, Butenandt O, Selzle D, Landthaler M

出版信息

Hautarzt. 1981 Feb;32(2):67-74.

PMID:7228665
Abstract

Two siblings (4 and 10 years old) with ichthyosis vulgaris, growth and mental retardation, hair dysplasia, teeth abnormalities, recurrent infections and malabsorption are presented. The elder sister of the children as well as the rest of the family are unremarkable. The complex of symptoms does not fit into one of the known Ichthyosis syndromes. Microscopically the dystrophic hairs show changes in diameters, nodules, lack of the medulla, rough cuticle and splits vertical to the axis, sometimes resembling trichorrhexis nodosa. In the scanning electron-microscope there is a clear difference to Netherton's syndrome. The plasma concentrations of the vitamines A, B12 as well as of beta-carotines are low in spite of normal nutrition. During parenteral therapy with vitamin A and B12 symptoms ameliorate slightly.

摘要

相似文献

1
[Ichthyosis vulgaris, growth retardation, hair dysplasia, tooth abnormalities, immunologic deficiencies, psychomotor retardation and resorption disorders. Case report of 2 siblings].
Hautarzt. 1981 Feb;32(2):67-74.
2
[Trichothiodystrophy: progresssive manifestations].[毛发硫营养不良:进行性表现]
Ann Dermatol Venereol. 1999 Oct;126(10):703-7.
3
[Netherton's syndrome. Current aspects. Apropos of 9 cases].
Ann Dermatol Venereol. 1991;118(8):525-30.
4
[Trichothiodystrophy].毛发硫营养不良
Ann Dermatol Venereol. 1987;114(12):1529-36.
5
Tay or IBIDS syndrome. A case with growth and mental retardation, congenital ichthyosis and brittle hair.泰伊综合征或IBIDS综合征。一例伴有生长发育迟缓、先天性鱼鳞病和脆发的病例。
Acta Paediatr Scand. 1991 Dec;80(12):1241-5. doi: 10.1111/j.1651-2227.1991.tb11817.x.
6
Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?眼皮肤白化病、免疫缺陷、血液系统疾病及轻微异常:一种新的常染色体隐性综合征?
Am J Med Genet. 1994 Apr 15;50(3):224-7. doi: 10.1002/ajmg.1320500303.
7
[Ichthyosis vulgaris, deafness, pili torti and tooth abnormalities].
Hautarzt. 1978 May;29(5):276-80.
8
[Sjögren-Larsson syndrome. Study of 2 cases].
An Esp Pediatr. 1983 May;18(5):399-402.
9
Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.两名女性同胞患有一种此前未报道过的大脑中动脉/智力障碍综合征:产前和产后生长发育迟缓、虹膜缺损、痉挛、面部畸形和脑室扩张。
Genet Couns. 1999;10(3):265-9.
10
Ichthyosis linearis circumflexa comèl. A clinico-statistical approach to its relationship with Netherton's syndrome.
Dermatologica. 1974;149(4):201-9.

引用本文的文献

1
Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations.毛发硫营养不良:对112例已发表病例的系统评价描绘了广泛的临床表现谱。
J Med Genet. 2008 Oct;45(10):609-21. doi: 10.1136/jmg.2008.058743. Epub 2008 Jun 25.
2
Tay syndrome.泰伊综合征
Indian J Pediatr. 2008 Mar;75(3):288-90. doi: 10.1007/s12098-008-0062-1.
3
The Tay syndrome (congenital ichthyosis with trichothiodystrophy).泰伊综合征(先天性鱼鳞病伴毛发硫营养不良)。
Eur J Pediatr. 1984 Jan;141(3):147-52. doi: 10.1007/BF00443212.
4
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity.患有光敏感型毛发硫营养不良的患者存在着色性干皮病(互补组D)突变。
Hum Genet. 1986 Oct;74(2):107-12. doi: 10.1007/BF00282072.
5
Trichothiodystrophy without photosensitivity. Biochemical, ultrastructural and DNA repair studies.无光敏性的毛发硫营养不良。生化、超微结构及DNA修复研究。
Eur J Pediatr. 1988 May;147(4):439-41. doi: 10.1007/BF00496431.
6
Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome.
Hum Genet. 1988 Jan;78(1):106-8. doi: 10.1007/BF00291250.
7
Professor Dr. Dr. h. c. Otto Braun-Falco.奥托·布劳恩-法尔科教授,医学博士、荣誉博士
Arch Dermatol Res. 1987;279 Suppl:S4-23. doi: 10.1007/BF00585915.