WordNet

of or relating to the cerebrum or brain; "cerebral hemisphere"; "cerebral activity"
involving intelligence rather than emotions or instinct; "a cerebral approach to the problem"; "cerebral drama" (同)intellectual
a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
of or relating to or forming or attached to a skeleton; "the skeletal system"; "skeletal bones"; "skeletal muscles"
(of muscular tissue) the state of being hypotonic (同)hypotonus, hypotonicity

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1. ダウン症：臨床的特徴および診断 down syndrome clinical features and diagnosis
2. 小児および思春期における肥満の定義、疫学および病因 definition epidemiology and etiology of obesity in children and adolescents
3. 微細欠失症候群（1番～11番染色体） microdeletion syndromes chromosomes 1 to 11
4. 知的障害（精神遅滞）をもつ成人のプライマリケア primary care of the adult with intellectual disability mental retardation
5. 筋力低下を呈する小児の病因および評価 etiology and evaluation of the child with muscle weakness

Walters-Sen LC1, Windemuth K1, Angione K1, Nandhlal J1, Milunsky JM2.
European journal of medical genetics.Eur J Med Genet.2015 May;58(5):305-9. doi: 10.1016/j.ejmg.2015.03.004. Epub 2015 Apr 6.
Submicroscopic duplications of 5p13 have been recently reported in several cases, warranting the description of a new clinical entity (Chromosome 5p13 Duplication Syndrome; MIM 613174). These microduplications, while variable in size, all contain at least part of the NIPBL gene. Patients with duplic
PMID 25858703

Magoulas PL1, El-Hattab AW.
Orphanet journal of rare diseases.Orphanet J Rare Dis.2012 Jan 4;7:2. doi: 10.1186/1750-1172-7-2.
Chromosome 15q24 microdeletion syndrome is a recently described rare microdeletion syndrome that has been reported in 19 individuals. It is characterized by growth retardation, intellectual disability, and distinct facial features including long face with high anterior hairline, hypertelorism, epica
PMID 22216833

Sone S1.
Brain & development.Brain Dev.1994 May-Jun;16(3):183-8.
In a follow-up study of 259 floppy infants of undetermined cause in my laboratory, 11 patients were later diagnosed as having the Prader-Willi syndrome (PWS). To clarify the pathogenesis of muscle hypotonia in PWS, I examined muscle biopsies by histochemical and morphometric methods and the results
PMID 7943601