Examples of using Ectodermal in English and their translations into Spanish
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Grid mapping ectodermal contours.
All ectodermal tissues are controlled from the cerebrum.
Epithelial cells derived from ectodermal cells.
Ectodermal cells become brain, skin and adrenal tissues;
HSV tend to infect cells of ectodermal origin.
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Ectodermal dysplasia, a clinical case and review of the literature.
There are many different types of ectodermal dysplasias.
In some congenital ectodermal dysplasias, patients have no nails(anonychia).
The breasts are secondary reproductive glands of ectodermal origin.
The Hypohidrotic ectodermal dysplasia is one of about 150 types of ectodermal dysplasia.
They occur as such, orin association with other congenital ectodermal defects.
Signs and symptoms of Hypohidrotic ectodermal dysplasia include hipohidrosis, hipotricosis and hypodontia.
This registry is an international registry and includes all ectodermal dysplasia subtypes.
The Ectodermal Dysplasias International Registry is currently the only official ectodermal dysplasias registry.
This registry has been created specifically for individuals affected by ectodermal dysplasias.
The anomaly of the apical ectodermal ridge, which helps direct development of the extremities, may also be involved in this process.
They have identified more than 80 mutations in the EDA gene in people with Hypohidrotic ectodermal dysplasia.
It is especially important for the normal development of ectodermal, such as skin, hair, teeth and nails structures.
It is differentiated from the rectum by the transition of the internal surface from endodermal to skinlike ectodermal tissue.
However, it is unclear how these changes result in an abnormal ectodermal development and specific features of the syndrome.
Mutations in the gene cause EDA X- linked form of the disease,which represents 95% of all cases of hypohidrotic ectodermal dysplasia.
They have identified more than 90 mutations in the AIRE gene in people with ectodermal dystrophy, candidiasis, autoimmune polyendocrinopathy APECED.
Ectodermal dystrophy, candidiasis, autoimmune polyendocrinopathy(APECED), also known as APS type 1 or type 1 autoimmune polyendocrinopathy syndrome is a hereditary disease that affects many organs.
These genetic changes alter signaling pathway necessary for the formation of ectodermal structures such as hair follicles and sweat glands.
As a result, the receiver can not probably trigger the necessary signals for the ectoderm-mesoderm interactions and normal development of hair follicles, sweat glands,and other ectodermal structures.
Fit for the diagnosis of white spot disease in target tissues(Shrimp tissue of ectodermal and mesodermal origin) of Litopenaeus vannamei and for the following purposes.
Consequently, the receiver is not available for chemical trigger signals required for mesoderm andectoderm-normal development of ectodermal structures interactions.
The mutation in the gene responsible EDARADD hypohidrotic ectodermal dysplasia replaces the amino acid glutamine for lysine at amino acid position 142 of the protein Glu142Lys.
The cardiofaciocutaneous Cutaneous(CFC) syndrome is a multisystem congenital disorder characterized by its association with several characteristic abnormalities(heart,facial and ectodermal) and mental retardation.
For its part,the abnormal development of tissues in people with ectodermal dysplasia craneoectodérmica can generate wispy hair, small or missing teeth, nails short and sagging skin.