Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 163 for Growth failure
  1. Isolated growth hormone deficiency 
    ... all the types. In people with type IA, growth failure is evident in infancy as affected babies are ... IB is characterized by short stature, but this growth failure is typically not as severe as in type ...
    https://medlineplus.gov/.../isolated-growth-hormone-deficiency - Genetics
  2. SHOX gene 
    ... SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of ... short stature homeobox) are an important cause of growth failure in children with short stature. J Clin Endocrinol ...
    https://medlineplus.gov/genetics/gene/shox - Genetics
  3. GH1 gene 
    ... isolated growth hormone deficiency type IA and severe growth failure by age 6 months. GH1 gene mutations that cause type IB are found throughout the gene and allow some growth hormone to be produced.Most GH1 gene mutations ...
    https://medlineplus.gov/genetics/gene/gh1 - Genetics
  4. Léri-Weill dyschondrosteosis 
    ... SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity. J Clin Endocrinol Metab. 2004 Sep;89(9):4403-8. doi: ... Citation on PubMed
    https://medlineplus.gov/.../condition/leri-weill-dyschondrosteosis - Genetics
  5. Glycogen storage disease type 0 
    ... years, or they can include developmental delay and growth failure. The prevalence of GSD 0 is unknown; fewer ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  6. X-linked severe combined immunodeficiency 
    X-linked severe combined immunodeficiency (SCID) is an inherited disorder of the immune system that occurs almost exclusively in males. Children with X- ...
    https://medlineplus.gov/...x-linked-severe-combined-immunodeficiency - Genetics
  7. Yuan-Harel-Lupski syndrome 
    Yuan-Harel-Lupski (YUHAL) syndrome is a rare neurological condition that has a combination of features of two other disorders, Potocki-Lupski syndrome and ...
    https://medlineplus.gov/.../condition/yuan-harel-lupski-syndrome - Genetics
  8. Potocki-Lupski syndrome 
    ... gain weight at the expected rate (described as failure to thrive), and children with this condition tend to be ... a microduplication syndrome associated with oropharyngeal dysphagia and failure to thrive. J Pediatr. 2011 Apr;158(4):655-659. ...
    https://medlineplus.gov/genetics/condition/potocki-lupski-syndrome - Genetics
  9. Congenital sucrase-isomaltase deficiency 
    ... gain weight and grow at the expected rate (failure to thrive) and malnutrition. The prevalence of congenital sucrase-isomaltase ... Schwartz ID. Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis. BMC Pediatr. 2002 Apr 25; ...
    https://medlineplus.gov/.../congenital-sucrase-isomaltase-deficiency - Genetics
  10. RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy 
    ... grow or gain weight at the expected rate (failure to thrive). Many have a smaller-than-normal head size ( ... vomiting, and diarrhea and can contribute to a failure to thrive. Less commonly, individuals with RRM2B-MDS develop seizures ...
    https://medlineplus.gov/...halomyopathic-form-with-renal-tubulopathy - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next