ハーバー症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- German chemist noted for the synthetic production of ammonia from the nitrogen in air (1868-1934) (同)Fritz Haber
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2018/03/06 19:46:41」(JST)
[Wiki en表示]
Haber syndrome |
Classification and external resources |
DiseasesDB |
31372 |
[edit on Wikidata]
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Haber syndrome is a cutaneous disorder of hyperpigmentation characterized by reticulated pigmentation of the person's skin.[1] A rare genodermatosis,[2] its key features include "rosacea-like facial eruption[,] reticulated hyperpigmentation of major flexures, comedones on the back and neck, and pitted facial scars."[1]
See also
- List of cutaneous conditions
References
- ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 955. ISBN 1-4160-2999-0.
- ^ McCormack, CJ; Cowen P. (May 1997). "Haber's syndrome". Australas. J. Dermatol. U.S. National Library of Medicine. 38 (2): 82–4. PMID 9159964.
Pigmentation disorders/Dyschromia (L80–L81, 709.0)
|
Hypo-/
leucism |
Loss of
melanocytes |
Vitiligo |
- Quadrichrome vitiligo
- Vitiligo ponctué
|
Syndromic |
- Alezzandrini syndrome
- Vogt–Koyanagi–Harada syndrome
|
Melanocyte
development |
- Piebaldism
- Waardenburg syndrome
- Tietz syndrome
|
|
Loss of melanin/
amelanism |
Albinism |
- Oculocutaneous albinism
- Ocular albinism
|
Melanosome
transfer |
- Hermansky–Pudlak syndrome
- Chédiak–Higashi syndrome
- Griscelli syndrome
- Elejalde syndrome
- Griscelli syndrome type 2
- Griscelli syndrome type 3
|
Other |
- Cross syndrome
- ABCD syndrome
- Albinism–deafness syndrome
- Idiopathic guttate hypomelanosis
- Phylloid hypomelanosis
- Progressive macular hypomelanosis
|
|
Leukoderma w/o
hypomelanosis |
- Vasospastic macule
- Woronoff's ring
- Nevus anemicus
|
Ungrouped |
- Nevus depigmentosus
- Postinflammatory hypopigmentation
- Pityriasis alba
- Vagabond's leukomelanoderma
- Yemenite deaf-blind hypopigmentation syndrome
- Wende–Bauckus syndrome
|
|
Hyper- |
Melanin/
Melanosis/
Melanism |
Reticulated |
- Dermatopathia pigmentosa reticularis
- Pigmentatio reticularis faciei et colli
- Reticulate acropigmentation of Kitamura
- Reticular pigmented anomaly of the flexures
- Naegeli–Franceschetti–Jadassohn syndrome
- Dyskeratosis congenita
- X-linked reticulate pigmentary disorder
- Galli–Galli disease
- Revesz syndrome
|
Diffuse/
circumscribed |
- Lentigo/Lentiginosis: Lentigo simplex
- Liver spot
- Centrofacial lentiginosis
- Generalized lentiginosis
- Inherited patterned lentiginosis in black persons
- Ink spot lentigo
- Lentigo maligna
- Mucosal lentigines
- Partial unilateral lentiginosis
- PUVA lentigines
- Melasma
- Erythema dyschromicum perstans
- Lichen planus pigmentosus
- Café au lait spot
- Poikiloderma (Poikiloderma of Civatte
- Poikiloderma vasculare atrophicans)
- Riehl melanosis
|
Linear |
- Incontinentia pigmenti
- Scratch dermatitis
- Shiitake mushroom dermatitis
|
Other/
ungrouped |
- Acanthosis nigricans
- Freckle
- Familial progressive hyperpigmentation
- Pallister–Killian syndrome
- Periorbital hyperpigmentation
- Photoleukomelanodermatitis of Kobori
- Postinflammatory hyperpigmentation
- Transient neonatal pustular melanosis
|
|
Other
pigments |
Iron |
- Hemochromatosis
- Iron metallic discoloration
- Pigmented purpuric dermatosis
- Schamberg disease
- Majocchi's disease
- Gougerot–Blum syndrome
- Doucas and Kapetanakis pigmented purpura/Eczematid-like purpura of Doucas and Kapetanakis
- Lichen aureus
- Angioma serpiginosum
- Hemosiderin hyperpigmentation
|
Other
metals |
- Argyria
- Chrysiasis
- Arsenic poisoning
- Lead poisoning
- Titanium metallic discoloration
|
Other |
- Carotenosis
- Tattoo
- Tar melanosis
|
|
|
Dyschromia |
- Dyschromatosis symmetrica hereditaria
- Dyschromatosis universalis hereditaria
|
See also |
- Skin color
- Skin whitening
- Tanning (Sunless)
|
UpToDate Contents
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English Journal
- Caffeine Impact on Metabolic Syndrome Components Is Modulated by a CYP1A2 Variant.
- Platt DE1, Ghassibe-Sabbagh M, Salameh P, Salloum AK, Haber M, Mouzaya F, Gauguier D, Al-Sarraj Y, El-Shanti H, Zalloua PA, Abchee AB.
- Annals of nutrition & metabolism.Ann Nutr Metab.2016;68(1):1-11. doi: 10.1159/000441481. Epub 2015 Nov 21.
- Cultural, dietary, and lifestyle factors are the main modulators of type 2 diabetes mellitus (T2DM) disease risk. Coffee is one of the most popular worldwide beverages, and recent epidemiological studies have showed that coffee consumption is associated with a lower risk of T2DM. This study investig
- PMID 26588584
- Accuracy of Endocrine Tests for Detecting Hypogonadotropic Hypogonadism in Girls.
- Binder G1, Schweizer R2, Haber P2, Blumenstock G3, Braun R2.
- The Journal of pediatrics.J Pediatr.2015 Sep;167(3):674-8.e1. doi: 10.1016/j.jpeds.2015.05.039. Epub 2015 Jun 18.
- OBJECTIVE: To assess the accuracy of inhibin B and the gonadotropin releasing hormone agonist test for the diagnosis of hypogonadotropic hypogonadism (HH).STUDY DESIGN: We performed a retrospective analysis of data collected 2009-2014 using a strict clinical protocol. All prepubertal nonunderweight
- PMID 26095287
- Post-Licensure Surveillance of Trivalent Live-Attenuated Influenza Vaccine in Children Aged 2-18 Years, Vaccine Adverse Event Reporting System, United States, July 2005-June 2012.
- Haber P1, Moro PL1, Cano M1, Vellozzi C1, Lewis P1, Woo EJ2, Broder K1.
- Journal of the Pediatric Infectious Diseases Society.J Pediatric Infect Dis Soc.2015 Sep;4(3):205-13. doi: 10.1093/jpids/piu034. Epub 2014 May 7.
- BACKGROUND: The first trivalent live-attenuated influenza vaccine (LAIV3) was licensed in 2003 for use in healthy persons 5-49 years of age. In 2007, the US Food and Drug Administration expanded its indication to healthy children 2-4 years of age.METHODS: We searched the Vaccine Adverse Event Report
- PMID 26407428
Japanese Journal
- Kindler syndrome. Clinical and ultrastructural findings
- The broad spectrum of Dowling Degos disease including Haber's syndrome, -A hereditary abnormal reactivity to stimulation, increasing with age?-Case reports and management
- The Bloch-Sulzberger Syndrome Incontinentia Pigmenti (Incontinentia Pigmenti)
Related Links
- Definition of Haber syndrome in the Medical Dictionary. Haber syndrome explanation. Information about Haber syndrome in Free online English dictionary. What is Haber syndrome? Meaning of Haber syndrome medical term. What ...
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★リンクテーブル★
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- 英
- Haber syndrome
- 同
- 屈曲部網状色素異常 reticular pigmented anomaly of flexures
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