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Genetic genealogy / Medical genetics / Mental retardation / RPS6KA3 / X-linked mental retardation / Sensorineural hearing loss / Rare diseases / Ciliopathy / Fryns Syndrome / Health / Syndromes / Coffin–Lowry syndrome


Coffin-Lowry Syndrome The Coffin–Lowry syndrome (CLS) (MIMis a syndromic form of X-linked mental retardation characterized in male patients by psychomotor retardation, growth retardation, and various skeletal
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Document Date: 2015-05-13 15:34:29


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City

Hoboken / Young / /

Company

Hunter AG / Siris E. & Wegenkia L.C. / Temtamy S.A. / /

MedicalCondition

loss of consciousness / cranial hyperostosis / microcephaly / drop attacks / non syndromic X-linked mental retardation / RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome / sensorineural hearing loss / mitral valve dysfunction / pneumonia / mental retardation / injury / Obesity / spinal kyphosis/scoliosis / Lowry syndrome / schizophrenia / disease / Epilepsy / Coffin-Lowry syndrome / hypotonia / dominant gene mental retardation syndrome / psychiatric illness / only non-syndromic mental retardation / myocarditis / convulsion / depression / X-linked mental retardation / inherited faciodigital mental retardation syndrome / orbital hypertelorism / epileptic seizures / /

Person

André Hanauer / /

Product

clonazepam / /

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