WordNet

filamentous hairlike growth on a plant; "peach fuzz" (同)fuzz, tomentum
a filamentous projection or process on an organism
any of the cylindrical filaments characteristically growing from the epidermis of a mammal; "there is a hair in my soup" (同)pilus
a covering for the body (or parts of it) consisting of a dense growth of threadlike structures (as on the human head); helps to prevent heat loss; "he combed his hair"; "each hair consists of layers of dead keratinized cells"
an impairment of health or a condition of abnormal functioning
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

PrepTutorEJDIC

〈C〉(人間・動物の1本の)『毛』;(植物・昆虫などの)毛 / 〈U〉《集合的に》『髪の毛』,毛,毛髪;(動物の)体毛 / 《a~》1本の毛ほどの量(距離,程度),ごくわずか
(体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
女性の話術芸人 =diseur
病気にかかった / 病的な,不健全な(morbid)
おや,はああ,ああ(驚き・喜び・疑い・ためらいなどを表す声)
hectare; hectares

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/12/12 15:05:19」(JST)

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[Wiki en表示]

Hair diseases are disorders primarily associated with the follicles of the hair.

An example is hypertrichosis.

Many hair diseases can be associated with distinct underlying disorders.

Piedra are fungal diseases.

External links

http://www.nlm.nih.gov/medlineplus/hairdiseasesandhairloss.html

This article about a disease, disorder, or medical condition is a stub. You can help Wikipedia by expanding it.

UpToDate Contents

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1. 脱毛の評価および診断 evaluation and diagnosis of hair loss
2. 軟骨毛髪形成不全症 cartilage hair hypoplasia
3. Fox-Fordyce disease (apocrine miliaria)
4. 頭部白癬 tinea capitis
5. 下肢末梢動脈疾患の臨床的特徴および診断 clinical features and diagnosis of lower extremity peripheral artery disease

English Journal

Expression pattern of wolframin, the WFS1 (Wolfram syndrome-1 gene) product, in common marmoset (Callithrix jacchus) cochlea.

Suzuki N1, Hosoya M, Oishi N, Okano H, Fujioka M, Ogawa K.
Neuroreport.Neuroreport.2016 Aug 3;27(11):833-6. doi: 10.1097/WNR.0000000000000624.
Wolfram syndrome is an autosomal recessive disorder of the neuroendocrine system, known as DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness) syndrome, and considered an endoplasmic reticulum disease. Patients show mutations in WFS1, which encodes the 890 amino acid protein
PMID 27341211

SMARCE1, a rare cause of Coffin-Siris Syndrome: Clinical description of three additional cases.

Zarate YA1, Bhoj E2, Kaylor J1, Li D2, Tsurusaki Y3, Miyake N3, Matsumoto N3, Phadke S4, Escobar L5, Irani A5, Hakonarson H2, Schrier Vergano SA6.
American journal of medical genetics. Part A.Am J Med Genet A.2016 Aug;170(8):1967-73. doi: 10.1002/ajmg.a.37722. Epub 2016 Jun 5.
Coffin-Siris syndrome (CSS, MIM 135900), is a well-described, multiple congenital anomaly syndrome characterized by coarse facial features, hypertrichosis, sparse scalp hair, and hypo/aplastic digital nails and phalanges, typically of the 5th digits. Mutations in the BAF (SWI/SNF)-complex subunits (
PMID 27264197

[Langer-Giedion syndrome with 8q23.1-q24.12 deletion diagnosed by comparative genomic hybridization].

Ruiz-Botero F1, Pachajoa H2.
Archivos argentinos de pediatría.Arch Argent Pediatr.2016 Aug 1;114(4):e228-32. doi: 10.5546/aap.2016.e228. Epub 2016 Aug 1.
in

English, SpanishEl síndrome de Langer-Giedion, también conocido como síndrome tricorrinofalángico tipo II, es una enfermedad hereditaria multisistémica que pertenece al grupo de síndromes por deleción de genes contiguos. La causa de este síndrome es una deleción heterocigota que comp