| Entry |
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| Name |
Kosaki overgrowth syndrome |
| Description |
Kosaki overgrowth syndrome (KOGS) is a novel syndrome characterized by skeletal overgrowth. Moreover, various degrees of abnormalities of the connective tissue and central nervous system are also often present. It has been reported that gain-of-function mutations in PDGFRB cause this syndrome. PDGFRB encodes platelet-derived growth factor receptor-beta, which plays a critical role in cell growth.
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| Category |
Congenital malformation
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| Brite |
Human diseases in ICD-11 classification [BR:br08403]
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2C Overgrowth syndromes
H02872 Kosaki overgrowth syndrome
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| Gene |
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| Other DBs |
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| Reference |
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| Authors |
Takenouchi T, Kodo K, Yamazaki F, Nakatomi H, Kosaki K |
| Title |
Progressive cerebral and coronary aneurysms in the original two patients with Kosaki overgrowth syndrome. |
| Journal |
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| Reference |
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| Authors |
Takenouchi T, Yamaguchi Y, Tanikawa A, Kosaki R, Okano H, Kosaki K |
| Title |
Novel overgrowth syndrome phenotype due to recurrent de novo PDGFRB mutation. |
| Journal |
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| Reference |
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| Authors |
Takenouchi T, Okuno H, Kosaki K |
| Title |
Kosaki overgrowth syndrome: A newly identified entity caused by pathogenic variants in platelet-derived growth factor receptor-beta. |
| Journal |
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