| Silver–Russell syndrome | |
|---|---|
| Classification and external resources | |
| ICD-10 | Q87.1 (ILDS Q87.114) |
| ICD-9 | 759.89 |
| OMIM | 180860 |
| DiseasesDB | 11748 |
| MedlinePlus | 001209 |
| eMedicine | ped/2099 |
Silver-Russell dwarfism, also called Silver-Russell syndrome (SRS) or Russell-Silver syndrome (RSS) is a growth disorder occurring in approximately 1/50,000 to 1/100,000 births. 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 and is one of the few forms that is considered treatable in some cases.
There is no statistical significance of the syndrome occurring in males or females.
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Its exact cause is unknown, but present research points toward a genetic component, possibly following maternal genes.
It involves hypomethylation of H19 and IGF2.[1]
Although confirmation of a specific genetic marker is in a significant number of individuals, there are no tests to clearly determine if this is what a person has. The syndrome is usually caused by a maternal uniparental disomy (UPD) on chromosome 7, in 10% of the cases, which is an imprinting error where the person receives two copies of chromosome 7 from the mother (maternally inherited). As a 'syndrome' a diagnosis is typically given for children upon confirmation of the presence of several 'symptoms' listed below. [2] Symptoms are Intrauterine Growth Restriction (IUGR) combined with some of the following:
The caloric intake of children with RSS must be carefully controlled in order to provide the best opportunity for growth,[2] if the child is unable to tolerate oral feeding then enteral feeding may be used, such as the percutaneous endoscopic gastrostomy.
In children with limb-length differences or scoliosis, physiotherapy can alleviate the problems caused by these symptoms. In more severe cases, surgery to lengthen limbs may be required. To prevent aggravating posture difficulties children with leg length differences may require a raise in their shoe.
Growth hormone therapy is often prescribed as part of the treatment of RSS. The hormones are given by injection typically daily from the age of 2 years old through teenage years. It may be effective even when the patient does not have a Growth Hormone deficiency. Growth Hormone therapy has been shown to increase the rate of growth in patients [3] and consequently prompts 'catch up' growth. This may enable the child to begin their education at a normal height, improving their self-esteem and interaction with other children. The effect of growth hormone therapy on mature and final height is as yet uncertain[4]. There are some theories suggesting that the therapy also assists with muscular development and managing hypoglycemia.
It is named for Henry Silver and Alexander Russell.[5][6][7]
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