WordNet

having or involving or consisting of more than one part or entity or individual; "multiple birth"; "multiple ownership"; "made multiple copies of the speech"; "his multiple achievements in public life"; "her multiple personalities"; "a pineapple is a multiple fruit"
the product of a quantity by an integer; "36 is a multiple of 9"
a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
a focal growth that resembles a neoplasm but results from faulty development in an organ

PrepTutorEJDIC

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/06/19 21:47:40」(JST)

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. カウデン症候群などのPTEN過誤腫症候群 pten hamartoma tumor syndrome including cowden syndrome
2. 乳癌および卵巣癌の遺伝的感受性：次世代シークエンシングパネル inherited susceptibility to breast and ovarian cancer next generation sequencing panels
3. 表皮母斑および表皮母斑症候群 epidermal nevus and epidermal nevus syndrome
4. 甲状腺結節および非髄様甲状腺癌におけるオンコジーンおよび腫瘍抑制遺伝子 oncogenes and tumor suppressor genes in thyroid nodules and nonmedullary thyroid cancer
5. 子宮平滑筋腫（子宮筋腫）の変異型 variants of uterine leiomyomas fibroids

Beta-catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome"

Galatola M, Paparo L, Duraturo F, Turano M, Rossi GB, Izzo P, De Rosa M.AbstractABSTRACT:
BMC medical genetics.BMC Med Genet.2012 Apr 20;13(1):28. [Epub ahead of print]
ABSTRACT:BACKGROUND: The "PTEN hamartoma tumor syndrome" (PHTS) includes a group of syndromes caused by germline mutations within the tumor suppressor gene "phosphatase and tensin homolog deleted on chromosome ten" (PTEN), characterized by multiple polyps in the gastrointestinal tract and by a highl
PMID 22520842

Pulmonary cysts of Birt-Hogg-Dubé syndrome: a clinicopathologic and immunohistochemical study of 9 families.

Furuya M, Tanaka R, Koga S, Yatabe Y, Gotoda H, Takagi S, Hsu YH, Fujii T, Okada A, Kuroda N, Moritani S, Mizuno H, Nagashima Y, Nagahama K, Hiroshima K, Yoshino I, Nomura F, Aoki I, Nakatani Y.SourceDepartment of Molecular Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
The American journal of surgical pathology.Am J Surg Pathol.2012 Apr;36(4):589-600.
Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant disorder characterized by fibrofolliculomas, renal tumors, and pulmonary cysts with recurrent pneumothorax. Multiple pulmonary cysts and pneumothorax are the key signs for diagnosing BHD syndrome. The pathologic features of BHD pulmonary cysts,
PMID 22441547

Intradural Extramedullary Ganglioneuroma Associated With Multiple Hamartoma Syndrome

TEI Rinsei,MORIMOTO Tetsuya,MIYAMOTO Kazunori,AKETA Shuta,SHIMOKAWARA Tatsuo,SHIN Yasushi,HIRONAKA Yasuo
Neurologia medico-chirurgica 47(11), 513-515, 2007-11-15
… A 51-year-old woman presented with a rare completely intradural and extramedullary spinal ganglioneuroma associated with multiple hamartoma syndrome and manifesting as complaints of neck pain and dizziness persisting for 8 months. …
NAID 110006456088

HARADA NAOHIKO,SUGIMURA TAKASHI,YOSHIMURA RIE,MOTOMURA SEIJI,SHIRAHAMA SHUYA,NARAMOTO JUN-ICHI,CHIJIIWA YOSHIHARU,NAKAMURA KAZUHIKO,ITO KEN-ICHI,NAWATA HAJIME
Journal of gastroenterology 38(1), 87-91, 2003-01-01
NAID 50000736187