EEM Syndrome

EEM syndrome (or Ectodermal dysplasia, Ectrodactyly and Macular dystrophy syndrome) is an autosomal recessive congenital malformation disorder affecting tissues associated with the ectoderm (skin, hair, nails, teeth), and also the hands, feet and eyes.

Read more about EEM SyndromeCharacteristics, Pathophysiology

Other articles related to "eem syndrome":

EEM Syndrome - Pathophysiology
... EEM syndrome is caused by mutations in the P-cadherin gene (CDH3) ... responsible for the macular dystrophy and spectrum of malformations found in EEM syndrome, due in part to developmental errors caused by the resulting inability ... found on human chromosome 3) may also play a role in EEM syndrome ...

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    [T]he syndrome known as life is too diffuse to admit of palliation. For every symptom that is eased, another is made worse. The horse leech’s daughter is a closed system. Her quantum of wantum cannot vary.
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