Russell-Silver syndrome

Russell-Silver syndrome
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Can Russell-Silver syndrome be inherited?
Most cases of Russell-Silver syndrome are sporadic, which means they occur in people with no history of the disorder in their family.

Russell-Silver Syndrome is a very rare genetic disorder. Most cases of Russell-Silver Syndrome are the result of new genetic changes (mutations) that occur randomly for no apparent reason.

Russell-Silver syndrome
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Definition ...

Many individuals with Chromosome 15 Ring have some features similar to those associated with Russell-Silver syndrome (RSS), which is a genetic disorder characterized by growth deficiency and short stature, distinctive facial abnormalities, ...

Growth problems may be a feature of syndromes such as Cushing's syndrome, Turner syndrome, Down syndrome, Noonan syndrome, Russell-Silver syndrome and Prader-Willi syndrome.
Growth hormone deficiency.

Genetic conditions such as Down syndrome, Turner syndrome, Williams syndrome, Russell-Silver syndrome, and Noonan syndrome
Bone or skeletal disorders such as rickets or achondroplasia ...

Cleidocranial dysostosis
Crouzon syndrome
Hurler syndrome
Pfeiffer syndrome
Rubinstein-Taybi syndrome
Russell-Silver syndrome (Russell-Silver dwarf)
Use of the antiseizure drug trimethadione during pregnancy ...

phenotype - refers to the physical characteristics and abnormalities found in a person that are attributable to a specific disorder (for example, the phenotype for Russell-Silver Syndrome might include large forehead, triangular-shaped face, ...

Rubinstein Taybi syndrome
Russell-Silver syndrome see Silver-Russell syndrome
Russian Spring-summer Encephalitis see Arboviral Encephalitides
Ruvalcaba-Myhre-Smith syndrome see Bannayan-Riley-Ruvalcaba syndrome ...

See also: Growth hormone, Kidney, Symptom, Deficiency, Pregnancy