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Results 61 - 70 of 129 for Skeletal dysplasia
  1. Growth and Your 13-to 18-Year-Old (Nemours Foundation)  
    ... delays, delayed puberty, hypothyroidism, human growth hormone deficiency, skeletal dysplasias, malnutrition, general pediatrics, endocrinology, endocrine, adolescence, adolescent medicine, ...
    https://kidshealth.org/en/parents/growth-13-to-18.html - External Health Links
  2. Growth and Your 2- to 3-Year-Old (Nemours Foundation)  
    ... delays, delayed puberty, hypothyroidism, human growth hormone deficiency, skeletal dysplasias, malnutrition, general pediatrics, endocrinology, endocrine, CD1Endocrinology
    https://kidshealth.org/en/parents/growth-2-to-3.html - External Health Links
  3. About Microcephalic Osteodysplastic Primordial Dwarfism Type II (Nemours Foundation)  
    Dwarfism/Specifics ... Dwarfism ... Nemours Foundation ... A class of disorders where growth delay occurs at the earliest stages of development.
    https://www.nemours.org/.../about-primordial-dwarfism.html - External Health Links
  4. Gnathodiaphyseal dysplasia 
    ... to the fragile bones, jaw problems, and other skeletal abnormalities that occur in gnathodiaphyseal dysplasia. Researchers suggest that the mutations may affect the ...
    https://medlineplus.gov/.../condition/gnathodiaphyseal-dysplasia - Genetics
  5. Diastrophic dysplasia 
    ... bones from forming properly and resulting in the skeletal problems characteristic of diastrophic dysplasia. SLC26A2 This condition is inherited in an autosomal ...
    https://medlineplus.gov/genetics/condition/diastrophic-dysplasia - Genetics
  6. X-linked spondyloepiphyseal dysplasia tarda 
    ... are disproportionately long compared to their height.Other skeletal features of X-linked spondyloepiphyseal dysplasia tarda include an abnormality of the hip joint ...
    https://medlineplus.gov/...linked-spondyloepiphyseal-dysplasia-tarda - Genetics
  7. Atelosteogenesis type 2 
    ... type 2 are similar to those of another skeletal disorder called diastrophic dysplasia; however, atelosteogenesis type 2 is typically more severe. ... A, Superti-Furga A. Mutations in the diastrophic dysplasia sulfate transporter ... skeletal phenotypes, and diagnostic relevance. Hum Mutat. 2001 Mar; ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-2 - Genetics
  8. FGD1 gene 
    ... specific expression of Fgd1 during bone formation and skeletal defects in faciogenital dysplasia (FGDY; Aarskog syndrome). Dev Dyn. 2000 Aug;218( ...
    https://medlineplus.gov/genetics/gene/fgd1 - Genetics
  9. Terminal osseous dysplasia 
    Terminal osseous dysplasia is a disorder primarily involving skeletal abnormalities and certain skin changes. It is a member of a group of related conditions called otopalatodigital spectrum ...
    https://medlineplus.gov/.../condition/terminal-osseous-dysplasia - Genetics
  10. Spondyloperipheral dysplasia 
    ... the exception of the first (big) toes. Other skeletal abnormalities associated with spondyloperipheral dysplasia include short stature, shortened long bones of the ...
    https://medlineplus.gov/.../condition/spondyloperipheral-dysplasia - Genetics
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