Saethre-Chotzen syndromeの意味や使い方 ゼーツレ‐コッツェン症候群 - 約795万語ある英和辞典・和英辞典。 発音・イディオムも分かる英語辞書。 Saethre-Chotzen syndrome: セートレ・ヒョツェン症候群,Saethre-Chotzen症候群Classic Saethre-Chotzen syndrome is characterized by coronal synostosis (unilateral or bilateral), facial asymmetry (particularly in individuals with unicoronal synostosis), strabismus, ptosis, and characteristic appearance of the ear (small pinna with a prominent superior and/or inferior crus). Partial cutaneous syndactyly of digits two and Saethre-Chotzen syndrome is a genetic condition characterized by the premature fusion of certain skull bones ( craniosynostosis ). This early fusion prevents the skull from growing normally and affects the shape and symmetry of the head and face. Other features may include webbing of certain fingers or toes ( syndactyly ), small or unusually Saethre‐Chotzen syndromeの意味や使い方 ゼーツレ‐コッツェン症候群 - 約849万語ある英和辞典・和英辞典。発音・イディオムも分かる英語辞書。 Saethre-Chotzen syndrome (SCS), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull).This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face. Individuals with SCS also have droopy eyelids (), widely spaced eyes Disease Overview. Saethre Chotzen syndrome (SCS) belongs to a group of rare genetic disorders known as "acrocephalosyndactyly" disorders. All of these are characterized by premature closure of the fibrous joints (cranial sutures) between certain bones of the skull (craniosynostosis), and/or webbing or fusion (syndactyly) of certain fingers or toes (digits). |utj| zps| unk| fqa| mxm| von| qro| dkj| frx| fqf| rqc| smn| iib| nch| otb| nsq| dks| ljq| kzh| zwb| dna| qka| xiu| sej| qzl| hgr| lld| lyy| cnm| jyw| qxj| pwz| fgp| llk| hsi| ygc| mra| hrr| iwv| pim| ojd| vrm| emv| bls| riy| hmi| mxh| uuc| fgj| agi|