Silver–Russell syndrome

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(Redirected from Silver-Russell dwarfism)

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Silver–Russell syndrome
Synonyms Russell–Silver syndrome, SRS
Pronounce
Specialty Medical genetics
Symptoms Growth retardation, short stature, limb asymmetry, facial dysmorphism
Complications N/A
Onset Prenatal
Duration Lifelong
Types N/A
Causes Genetic
Risks
Diagnosis Clinical evaluation, genetic testing
Differential diagnosis Intrauterine growth restriction, Prader-Willi syndrome, Beckwith-Wiedemann syndrome
Prevention N/A
Treatment Growth hormone therapy, nutritional support, orthopedic management
Medication
Prognosis Variable, generally good with treatment
Frequency 1 in 30,000 to 1 in 100,000
Deaths


Silver–Russell syndrome (SRS), also known as Russell–Silver syndrome (RSS), is a rare congenital condition characterized by intrauterine growth restriction, postnatal growth retardation, and distinctive facial features. It was first described by Henry Silver and Alexander Russell in the 1950s.

Signs and Symptoms[edit]

Individuals with Silver–Russell syndrome typically present with:

Genetics[edit]

Silver–Russell syndrome is a genetically heterogeneous condition. The most common genetic abnormalities associated with SRS include:

Diagnosis[edit]

The diagnosis of Silver–Russell syndrome is primarily clinical, based on the characteristic features. Genetic testing can confirm the diagnosis by identifying the specific genetic abnormalities.

Management[edit]

Management of Silver–Russell syndrome involves a multidisciplinary approach, including:

Prognosis[edit]

The prognosis for individuals with Silver–Russell syndrome varies. With appropriate medical care and support, many individuals can lead relatively normal lives, although they may have short stature and other health issues.

See also[edit]

References[edit]

External Links[edit]

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