Coffin-Lowry症候群 (Coffin-Lowry syndrome CLS) 通常见于重度或极重度智能障碍的男性，但疾病症状程度较轻微的个案亦曾被报导。此症是由于位在X染色体短 ...

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

In 1966 Coffin, Siris, and Wegienka 1 described a syndrome in two unrelated boys that has become known as the Coffin-Lowry Syndrome (CLS). Our examination of both boys showed developmental ...

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 ...

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 ...

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 ...

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 ...

Starting with her nine-year-old son Gabriel in the center - who suffers from a rare genetic disorder called Coffin-Lowry Syndrome - she drew 70 colored ovals, each representing an area of care.

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 ...

There is no cure and no standard course of treatment for Coffin-Lowry syndrome. Treatment is symptomatic and supportive, and may include physical and speech therapy and educational services.

I have a beautiful six-year-old son named Curtis who lights up any room the minute he walks into it. Born on Valentine's Day a seemingly normal baby boy, he was a younger brother to Phoebe.