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Idiopathic Short Stature

2011
Idiopathic short stature is a condition in which the height of the individual is more than 2 SD below the corresponding mean height for a given age, sex, and population, and in whom no identifiable disorder is present. It can be subcategorized into familial and non-familial ISS, according to information on delay of puberty and bone age.
Meinolf Noeker   +2 more
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Spontaneous Adult Height in Idiopathic Short Stature

Hormone Research, 2008
Two hundred and thirty-six patients with idiopathic short stature (ISS) (184 m, 52 f) who presented at a mean age of 12.2 (range 2.8-17.5) years, a mean height of-2.16 standard deviation score (SDS), a mean target height (THT) of-0.27 SDS (m = 0, were reinvestigated at a mean age of 20.5 (range 18-24) years.
M B, Ranke   +4 more
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Genetic studies in idiopathic short stature

Current Opinion in Pediatrics, 2000
Idiopathic short stature (ISS) refers to a heterogeneous group of children with marked growth failure of unknown cause, and encompasses familial short stature and constitutional delay of growth. It has been postulated that specific genetic mutations may explain certain cases of growth failure.
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Psychological Functioning in Idiopathic Short Stature

Hormone Research in Paediatrics, 2011
Living with idiopathic short stature (ISS) may entail significant risks to psychological functioning and quality of life. Apparent inconsistency among study findings can be resolved if methodological differences among study designs are taken into account (i.e., definition of particular endpoints, sample selection from clinic or population, source of ...
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Treatment of children and adolescents with idiopathic short stature

Nature Reviews Endocrinology, 2013
Idiopathic short stature (ISS) is defined as shortness in childhood without a specific cause. ISS may be familial or nonfamilial and may be associated with or without delay of pubertal development. Treatment can be considered in an attempt to reduce the psychological burden caused by short stature in childhood and adult life.
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Growth Hormone Treatment of Idiopathic Short Stature

Hormone Research, 2008
Considerable controversy exists about the use of growth hormone (GH) treatment in short children without classical GH deficiency (idiopathic short stature or ISS). ISS is a multifactorial disorder with many potential causes rather than a single diagnostic entity, and it is in essence a diagnosis of exclusion.
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Growth Hormone Use in Children with Idiopathic Short Stature

Annals of Pharmacotherapy, 2004
OBJECTIVE: To review the indication, pharmacology, pharmacokinetics, efficacy, and adverse effects of recombinant human growth hormone in children with idiopathic short stature (ISS). DATA SOURCES: A MEDLINE search (1966–December 2003)
Karen L, Weise, Milap C, Nahata
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Normal Variant and Idiopathic Short Stature

2018
This chapter reviews normal variant short stature, comprised of both familial short stature (FSS) and constitutional delay of growth and puberty (CDGP), as well as idiopathic short stature (ISS). FSS and CDGP are physiologic variants of short stature without an organic cause. Although ISS is not a “normal variant” of short stature, as with FSS and CDGP
Penny M. Feldman, Mary M. Lee
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[Growth hormone and idiopathic short stature].

Annales d'endocrinologie, 2009
Idiopathic short stature is defined by height below 3rd percentile, in a child with normal birth height and weight, lack of dysmorphy, endocrine deficiency or systemic disease. Food and Drugs administration approved GH treatment in this indication in the United States, because it induces height gain, and sometimes may increase quality of life. There is
F, Castinetti, C, Fabre-Brue, T, Brue
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