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Results 1 - 10 of 164 for Abnormal embryonic development
  1. Congenital hepatic fibrosis 
    ... hepatic fibrosis is caused by problems in the development of the portal veins and bile ducts before birth. These problems include abnormal formation of embryonic structures called ductal plates. Each ductal plate is ...
    https://medlineplus.gov/.../condition/congenital-hepatic-fibrosis - Genetics
  2. X-linked acrogigantism 
    ... somatic variants, arise randomly in one cell during embryonic development. As cells continue to divide, only cells arising from the first abnormal cell will have the variant. Other affected males ...
    https://medlineplus.gov/genetics/condition/x-linked-acrogigantism - Genetics
  3. Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 
    ... somatic mutations, arise randomly in one cell during embryonic development. As cells continue to divide, only cells arising from the first abnormal cell will have the mutation. MEG-PMG-POLY- ...
    https://medlineplus.gov/...ogyria-polydactyly-hydrocephalus-syndrome - Genetics
  4. CHARGE syndrome 
    ... CHD7 gene lead to the production of an abnormal CHD7 protein that is broken down ... embryonic development likely cause the signs and symptoms of CHARGE ...
    https://medlineplus.gov/genetics/condition/charge-syndrome - Genetics
  5. CHD7 gene 
    ... these mutations lead to the production of an abnormal CHD7 protein that is broken ... embryonic development likely cause the signs and symptoms of CHARGE ...
    https://medlineplus.gov/genetics/gene/chd7 - Genetics
  6. SOX10 gene 
    ... prevent the gene from making any protein. An abnormal or missing SOX10 protein ... embryonic development. Missing enteric nerves in certain parts of the ...
    https://medlineplus.gov/genetics/gene/sox10 - Genetics
  7. DLL3 gene 
    ... Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis. J Med Genet. 2003 May;40(5):333-9. doi: 10.1136/jmg.40.5.333. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/dll3 - Genetics
  8. Coloboma 
    ... this condition are likely undiagnosed. Coloboma arises from abnormal development of the eye. During the second month of development before birth, a seam called the optic fissure (also known as the choroidal fissure or embryonic fissure) closes to form the structures of the ...
    https://medlineplus.gov/genetics/condition/coloboma - Genetics
  9. Primary ciliary dyskinesia 
    ... intestines, or spleen. These organs may be structurally abnormal or improperly ... development. The severity of heterotaxy varies widely among affected ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
  10. GNAS gene 
    ... AMP (cAMP). An excess of cAMP may trigger abnormal cell growth and lead to ... early in embryonic development. Cells with the mutated GNAS gene can be ...
    https://medlineplus.gov/genetics/gene/gnas - Genetics
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