Human Growth Foundation
About Human Growth Foundation
The Human Growth Foundation (HGF) is a national, voluntary, non-profit organization that was established in 1965. It is dedicated to expanding and accelerating medical research into growth and growth disorders. Composed of concerned parents, friends of children with growth problems, adults experiencing growth hormone deficiency, and interested health professionals, the Human Growth Foundation supports family education and service, public education, support for training of growth specialists and education of medical professionals. It conducts national education conferences, makes starter research grants to investigators, and coordinates Human Growth Month. The foundation also publishes informational pamphlets, booklets, and a monthly newsletter and serves as an information clearinghouse for families of children who have growth disorders.
Related Rare Diseases:
- Recessive Multiple Epiphyseal Dysplasia
- Schimke Immuno-Osseous Dysplasia
- Pseudoachondroplasia
- Megalocornea Intellectual Disability Syndrome
- Costello Syndrome
- Acromicric Dysplasia
- Trichorhinophalangeal Syndrome Type III
- Leri Pleonosteosis
- Meier-Gorlin Syndrome
- Weismann-Netter-Stuhl Syndrome
- Mulibrey Nanism
- Kenny-Caffey Syndrome
- Bannayan-Riley-Ruvalcaba Syndrome
- Chromosome 15 Ring
- Campomelic Syndrome
- SHORT Syndrome
- Floating Harbor Syndrome
- Ellis-Van Creveld Syndrome
- Jansen Type Metaphyseal Chondrodysplasia
- Weill Marchesani Syndrome
- Leri-Weill Dyschondrosteosis
- Achondrogenesis
- Dyggve Melchior Clausen syndrome
- Metatropic Dysplasia I
- Growth Hormone Deficiency
- Growth Hormone Insensitivity
- Marshall-Smith Syndrome
- Weaver Syndrome
- Kniest Dysplasia
- Trichorhinophalangeal Syndrome Type I
- Noonan Syndrome with Multiple Lentigines
- Robinow Syndrome
- Rothmund-Thomson Syndrome
- McKusick Type Metaphyseal Chondrodysplasia
- Hypochondroplasia
- Asphyxiating Thoracic Dystrophy
- Optic Nerve Hypoplasia
- Seckel Syndrome
- Diastrophic Dysplasia
- Noonan Syndrome
- Leprechaunism
- Russell-Silver Syndrome
- Conradi Hünermann Syndrome
- Dominant Multiple Epiphyseal Dysplasia
- Spondyloepiphyseal Dysplasia Tarda
- Cockayne Syndrome
- Bloom Syndrome
- Turner Syndrome
- Froelich Syndrome
- Achondroplasia
- Nanismo de Mulibrey
- Acondroplasia
- Acondrogénesis
- Síndrome de Russell-Silver
- Síndrome de Turner
- Froelich Syndrome
- Síndrome de Rothmund-Thomson
- Displasia espondiloepifisaria tardía ligada al cromosoma X
- Síndrome de Weaver
- Síndrome de Noonan
- Síndrome SHORT
- Imagawa-Matsumoto Syndrome
- Síndrome de Imagawa-Matsumoto
