lordosis

ヒップ痛み, 低身長, 母趾の変形, 背骨の湾曲

動悸, 脚の筋肉の低下, 足足の筋肉のけいれん, 運動の制限です

Limb-girdle muscular dystrophy or Erb's muscular dystrophy is a type of muscular dystrophy that includes Duchenne muscular dystrophy, Becker's muscular dystrophy, and a large number of rarer disorders. 

制限された胸の動き, 戻って揺れる

お辞儀を手足, 低身長, 異常歩行, 足の痛み

口蓋のギャップ, 大舌, 難易度がスピーチ。, 食欲不振

Pierre Robin syndrome (PRS) is a congenital sequence of abnormalities in humans that may occur either as a distinct syndrome or as part of another underlying disorder. ... 

異常歩行, 発達の遅れ, 貧しい人々の社会的スキル, 高血圧

Williams syndrome (also Williams-Beuren syndrome, sometimes called Pixieism) is a rare genetic disorder, occurring in fewer than 1 in 7,500 live births.It is characterized by a distinctive, "elvish" facial appearance, along with a low nasal bridge; an unusually cheerful demeanor and ease with strangers, coupled with unpredictably occurring negative outbursts; mental retardation coupled with unusual (for persons who are diagnosed as mentally retarded) language skills; a love for music; and cardiovascular problems, such as supravalvular aortic stenosis and transient hypercalcaemia. 

低身長, 心雑音, heart defect, heart murmur systolic

Ellis-van Creveld Syndrome (also called chondroectodermal dysplasia or mesoectodermal dysplasia) is a rare genetic disorder of the skeletal dysplasia type.It involves numerous anomalies including post-axial polydactyly, congenital heart defects (most commonly an atrial septal defect producing a common atrium, occurring in 60% of affected individuals), pre-natal tooth eruption, fingernail dysplasia, short-limbed dwarfism, short ribs, partial hare-lip, and malformation of the wrist bones (fusion of the hamate and capitate bones).