{"id":11215,"date":"2025-07-27T06:24:36","date_gmt":"2025-07-27T04:24:36","guid":{"rendered":"https:\/\/valintermed.com\/?p=11215"},"modified":"2025-07-27T06:24:36","modified_gmt":"2025-07-27T04:24:36","slug":"semeynaya-nizkoroslost-fss","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/family-low-fss\/","title":{"rendered":"Familial Short Stature (FSS)"},"content":{"rendered":"
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Familial short stature (FSS) is a genetic disorder characterized by short stature within a family, with growth parameters below the 3rd percentile for the corresponding age and sex cohort. FSS includes a group of hereditary disorders that are usually not accompanied by other somatic or endocrine pathologies, such as growth hormone deficiency or other diseases that lead to impaired normal growth. The underlying mechanism that causes this disorder is genetic predisposition, with most forms of the disease inherited in an autosomal recessive manner. It is important to note that FSS is not usually a sign of any systemic disease, and children with this condition often have normal physical and mental development.<\/p>\n

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