Say–Meyer syndrome
X-linked recessive disorder characterised by developmental delay / From Wikipedia, the free encyclopedia
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Say–Meyer syndrome is a rare X-linked genetic disorder that is mostly characterized as developmental delay. It is one of the rare causes of short stature. It is closely related with trigonocephaly (a misshapen forehead due to premature fusion of bones in the skull). People with Say–Meyer syndrome have impaired growth, deficits in motor skills development and mental state.[1][2]
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Say–Meyer syndrome | |
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Other names | Trigonocephaly-short stature-developmental delay syndrome |
Say–Meyer syndrome is inherited in an X-linked recessive manner. |
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It is suggested that it is from a X-linked transmission.[3]