Топ-100
  • Turner syndrome Turner syndrome

    Turner syndrome, also known 45,X, or 45,X0, is a genetic condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary...

  • Silver–Russell syndrome Silver–Russell syndrome

    Silver–Russell syndrome, also called Silver–Russell dwarfism or Russell–Silver syndrome is a growth disorder occurring in approximately 1/50.000 to 1/100.000...

  • Pseudoachondroplasia Pseudoachondroplasia

    Pseudoachondroplasia is an inherited disorder of bone growth. It is a genetic autosomal dominant disorder. It is generally not discovered until 2–3 years of ...

  • Parastremmatic dwarfism Parastremmatic dwarfism

    Parastremmatic dwarfism is a rare bone disease that features severe dwarfism, thoracic kyphosis, a distortion and twisting of the limbs, contractures of the ...

  • Midget Midget

    Midget is a term for a person of unusually short stature that is considered by some to be pejorative. While not a medical term, it has been applied to person...

  • Microcephalic osteodysplastic primordial dwarfism type II Microcephalic osteodysplastic primordial dwarfism type II

    Microcephalic osteodysplastic primordial dwarfism type II is a form of dwarfism associated with brain and skeletal abnormalities. It was characterized in 198...

  • MAGIC Foundation MAGIC Foundation

    The MAGIC foundation for childrens growth is an American non-profit organization which helps families of children diagnosed with a wide variety of different ...

  • Local gigantism Local gigantism

    Local gigantism or localised gigantism is a condition in which a certain part of the body acquires larger than normal size due to excessive growth of the ana...

  • Leri–Weill dyschondrosteosis Leri–Weill dyschondrosteosis

    Leri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs and a bayonet-...

  • Kowarski syndrome Kowarski syndrome

    Kowarski syndrome describes cases of growth failure, despite the presence of normal or slightly high blood growth hormone by radioimmunoassay and low serum I...

  • Hypochondroplasia Hypochondroplasia

    Hypochondroplasia is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene that results in ...

  • Human Growth Foundation Human Growth Foundation

    The Human Growth Foundation is a nonprofit group that works with people with growth deficiencies. It is financed mainly by Genentech and Caremark. In 1994 it...

  • Growth hormone deficiency Growth hormone deficiency

    Growth hormone deficiency is a medical condition due to not enough growth hormone. Generally the most noticeable symptom is a short height. In newborns there...

  • Brooke Greenberg Brooke Greenberg

    Brooke Megan Greenberg was an American who remained physically and cognitively similar to a toddler, despite her increasing age. She was about 30 in tall, we...

  • Gigantism Gigantism

    Gigantism, also known as giantism, is a condition characterized by excessive growth and height significantly above average. In humans, this condition is caus...

  • Dwarfism Dwarfism

    Dwarfism, also known as short stature, occurs when an organism is extremely small. In humans, it is sometimes defined as an adult height of less than 147 cen...

  • Adiposogenital dystrophy Adiposogenital dystrophy

    Adiposogenital dystrophy is a condition which may be caused by tertiary hypogonadism originating from decreased levels in GnRH. Low levels of GnRH has been a...

  • Acromegaly Acromegaly

    Acromegaly is a disorder that results from excess growth hormone after the growth plates have closed. The initial symptom is typically enlargement of the han...

  • Achondroplasia Achondroplasia

    Achondroplasia is a genetic disorder that results in dwarfism. In those with the condition, the arms and legs are short, while the torso is typically of norm...

Growth disorders

Growth hormone therapy refers to the use of growth hormone GH as a prescription medication - it is one form of hormone therapy. Growth hormone is a peptide
the growth disorder proves deleterious, making it the opposite of heterosis or hybrid vigour. Hybrid growth disorders may be referred to as a growth dysplasia
December 2017. Growth Hormone Deficiency NORD National Organization for Rare Disorders 2016. Retrieved 12 December 2017. isolated growth hormone deficiency
Those with genetic disorders can sometimes be treated with surgery or physical therapy. Hormone disorders can also be treated with growth hormone therapy
INN is used as a prescription drug to treat children s growth disorders and adult growth hormone deficiency. In the United States, it is only available
Disorders 138 1 2 149 152. doi: 10.1016 j.jad.2011.11.046. ISSN 0165 - 0327. PMC 4479259. PMID 22305430. Levi - Montalcini R 2004 The nerve growth
food it may be more prone to metabolic disorders such as obesity and type II diabetes. In sheep, intrauterine growth restriction can be caused by heat stress
MUscle - LIver - BRain - EYe nanism is a rare autosomal recessive congenital disorder It causes severe growth failure along with abnormalities of the heart, muscle, liver
relationship between posttraumatic growth and symptoms of posttraumatic distress disorder PDF Journal of Anxiety Disorders 28 2 223 9. doi: 10.1016 j
intake disorder ARFID where people have a lack of interest in food and a group of other specified feeding or eating disorders Anxiety disorders depression
A growth chart is used by pediatricians and other health care providers to follow a child s growth over time. Growth charts have been constructed by observing

Stunted growth is a reduced growth rate in human development. It is a primary manifestation of malnutrition or more precisely undernutrition and recurrent
neurodevelopmental disorders tend to last for a person s entire lifetime. Neurodevelopmental disorders are impairments of the growth and development of
National Cooperative Growth Study NCGS is the largest observational database in the U.S. of children with growth disorders Started in 1985, NCGS was
proven to be difficult. Gigantism is the primary example of growth hormone hyper - secretion disorders a group of illnesses that are not yet deeply understood
Physiological disorders are distinguished from plant diseases caused by pathogens, such as a virus or fungus. While the symptoms of physiological disorders may
cause any developmental delays. Feeding disorders resemble failure to thrive, except that at times in feeding disorder there is no medical or physiological
Adrenal gland disorders or diseases are conditions that interfere with the normal functioning of the adrenal glands. Adrenal disorders may cause hyperfunction
disorders perform actions, tasks, and activities. Audiologist Health care professional who is trained to evaluate hearing loss and related disorders
soft tissue rheumatic disorders is used to describe these conditions. Rozman, P Bolta, M December 2007 Use of platelet growth factors in treating
Compensatory growth known as catch - up growth and compensatory gain, is an accelerated growth of an organism following a period of slowed development
results when the anterior pituitary gland produces excess growth hormone GH A number of disorders may increase the pituitary s GH output, although most
Fetal alcohol spectrum disorders FASDs are a group of conditions that can occur in a person whose mother drank alcohol during her pregnancy. Problems
Orofacial myofunctional disorders OMD sometimes called oral myofunctional disorder and tongue thrust are muscle disorders of the face, mouth, lips

Russell - Silver syndrome, thyroid disorders both congenital and acquired optic nerve hypoplasia, and other rare disorders MAGIC offers a national educational
per cent of work - related back disorders and improving job control can reduce 37 - 84 per cent of work - related wrist disorders Because workers maintain the
single episode. Many disorders have been described, with signs and symptoms that vary widely between specific disorders Such disorders may be diagnosed by
and heterozygotes according to the Hardy - Weinberg ratio. A series of growth disorders can occur at the cellular level and these consequently underpin much
Wajnrajch MP Dec 2002 Growth Hormone Releasing Hormone GHRH and the GHRH Receptor Reviews in Endocrine Metabolic Disorders 3 4 313 23. doi: 10
Mental disorders diagnosed in childhood are divided into two categories: childhood disorders and learning disorders These disorders are usually first

Achondroplasia

Achondroplasia is a genetic disorder that results in dwarfism. In those with the condition, the arms and legs are short, while the torso is typically of norm...

Achondroplasia in children

Achondroplasia in children is the most common form of dwarfism; it accounts for about 70% of all cases of dwarfism. Achondroplasia falls into the category of...

Acromegaly

Acromegaly is a disorder that results from excess growth hormone after the growth plates have closed. The initial symptom is typically enlargement of the han...

Adiposogenital dystrophy

Adiposogenital dystrophy is a condition which may be caused by tertiary hypogonadism originating from decreased levels in GnRH. Low levels of GnRH has been a...

Dwarfism

Dwarfism, also known as short stature, occurs when an organism is extremely small. In humans, it is sometimes defined as an adult height of less than 147 cen...

Gigantism

Gigantism, also known as giantism, is a condition characterized by excessive growth and height significantly above average. In humans, this condition is caus...

Brooke Greenberg

Brooke Megan Greenberg was an American who remained physically and cognitively similar to a toddler, despite her increasing age. She was about 30 in tall, we...

Growth hormone deficiency

Growth hormone deficiency is a medical condition due to not enough growth hormone. Generally the most noticeable symptom is a short height. In newborns there...

Hemihypertrophy

Hemihypertrophy, now more commonly referred to as hemihyperplasia in the medical literature, is a condition in which one side of the body or a part of one si...

Human Growth Foundation

The Human Growth Foundation is a nonprofit group that works with people with growth deficiencies. It is financed mainly by Genentech and Caremark. In 1994 it...

Hypochondroplasia

Hypochondroplasia is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene that results in ...

Kowarski syndrome

Kowarski syndrome describes cases of growth failure, despite the presence of normal or slightly high blood growth hormone by radioimmunoassay and low serum I...

Leri–Weill dyschondrosteosis

Leri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs and a bayonet-...

Local gigantism

Local gigantism or localised gigantism is a condition in which a certain part of the body acquires larger than normal size due to excessive growth of the ana...

Macrodystrophia lipomatosa

Macrodystrophia lipomatosa is a rare congenital disorder characterized by localised overgrowth of a part of an extremity or less commonly a whole extremity. ...

MAGIC Foundation

The MAGIC foundation for childrens growth is an American non-profit organization which helps families of children diagnosed with a wide variety of different ...

Mesomelia

Mesomelia refers to conditions in which the middle parts of limbs are disproportionately short. When applied to skeletal dysplasias, mesomelic dwarfism descr...

Microcephalic osteodysplastic primordial dwarfism type II

Microcephalic osteodysplastic primordial dwarfism type II is a form of dwarfism associated with brain and skeletal abnormalities. It was characterized in 198...

Midget

Midget is a term for a person of unusually short stature that is considered by some to be pejorative. While not a medical term, it has been applied to person...

Neotenic complex syndrome

Neotenic complex syndrome is a syndrome that presents as an extreme form of developmental delay, with the defining characteristic being neoteny of the patien...

Parastremmatic dwarfism

Parastremmatic dwarfism is a rare bone disease that features severe dwarfism, thoracic kyphosis, a distortion and twisting of the limbs, contractures of the ...

Pseudoachondroplasia

Pseudoachondroplasia is an inherited disorder of bone growth. It is a genetic autosomal dominant disorder. It is generally not discovered until 2–3 years of ...

Psychosocial short stature

Psychosocial short stature is a growth disorder that is observed between the ages of 2 and 15, caused by extreme emotional deprivation or stress. The symptom...

Seckel syndrome

Seckel syndrome, or microcephalic primordial dwarfism is an extremely rare congenital nanosomic disorder. Inheritance is autosomal recessive. It is character...

Silver–Russell syndrome

Silver–Russell syndrome, also called Silver–Russell dwarfism or Russell–Silver syndrome is a growth disorder occurring in approximately 1/50.000 to 1/100.000...

Turner syndrome

Turner syndrome, also known 45,X, or 45,X0, is a genetic condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary...