Russell Silver Syndrome | search
Click here to view Russell Silver Syndrome news from 60+ newspapers.
Bookmark or Share- Russell Silver Syndrome — MAGIC Foundation for Children's GrowthRussell-Silver syndrome (or Silver-Russell syndrome) is a rare genetic disorder characterized by delayed growth in-utero (IUGR) that spares head growth (meaning the newborn has a head size that is large for his body) and ongoing postnatal growth failure.
- Russell-Silver Syndrome: Symptoms, Causes, Diagnosis & OutlookRussell-Silver syndrome is a rare genetic condition that affects an estimated one in every 15,000 to 100,000 births. The exact frequency of the condition is unknown. Russell-Silver syndrome characteristics often resemble those of other growth disorders and congenital conditions.
- Silver–Russell syndrome - WikipediaSilver–Russell syndrome, also called Silver–Russell dwarfism, is a rare congenital growth disorder. In the United States it is usually referred to as Russell–Silver syndrome, and Silver–Russell syndrome elsewhere. It is one of 200 types of dwarfism and one of five types of primordial dwarfism.
- Russell-Silver Syndrome - Symptoms, Causes, Treatment | NORDRussell-Silver syndrome (RSS) is a rare disorder characterized by intrauterine growth restriction (IUGR), poor growth after birth, a relatively large head size, a triangular facial appearance, a prominent forehead (looking from the side of the face), body asymmetry and significant feeding difficulties.
- Russell Silver Syndrome: Causes, Symptoms and Diagnosis - HealthlineWhat Is Russell-Silver Syndrome? Russell-Silver syndrome (RSS), sometimes called Silver-Russell syndrome (SRS), is a congenital condition. It is characterized by stunted growth and limb or...
More
