What is Coffin-Lowry Syndrome? Coffin-Lowry Syndrome (CLS) is a genetic disorder (rare) characterized by intellectual disabilities and abnormalities in the head and face. Further, it is ...

Coffin–Lowry syndrome is an X-linked semidominant syndrome characterized typically by severe psychomotor and growth retardation, facial dysmorphism, digit abnormalities, and progressive skeletal ...

Q: Which doctor should I consult for Coffin-Lowry syndrome? A: For this syndrome, a well-qualified, experienced and trained physician in the field of genetics needs to be consulted. In addition ...

The Coffin-Lowry syndrome (CLS) is a syndromic form of X-linked mental retardation characterised in male patients by psychomotor and growth retardation, and various skeletal anomalies. CLS is ...

Most people wouldn’t recognize it as the symbol of the Coffin-Lowry syndrome Foundation, but the image is very meaningful for the Newark couple. Three of their four children, Quinten ...

Hildembrand's son, Mathis, has a rare genetic disorder known as Coffin-Lowry syndrome. According to the National Institute of Neurological Disorders and Stroke, Coffin-Lowry syndrome is a rare ...

What is Coffin-Lowry Syndrome? Coffin-Lowry Syndrome is a rare genetic disorder affecting several parts of the body. It is characterized by skeletal anomalies, intellectual disability and episodes ...

Coffin-Lowry syndrome (CLS) is a rare genetic condition that typically causes intellectual disability in infants. Physical symptoms of CLS may also include certain head and facial characteristics ...