ectodermal dysplasia sentence in Hindi
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- In Hay Wells syndrome, and other ectodermal dysplasia disorders, a missense, nonsense, or insertion mutation has occurred in the TP63 gene.
- "' Ectodermal dysplasia "'is not a single disorder, but a group of syndromes all deriving from abnormalities of the ectodermal structures.
- The suit was donated under an agreement between the Johnson Space Center and the Hampton, Va .-based Hypohidrotic Ectodermal Dysplasia Foundation.
- People with Naegeli Franceschetti Jadassohn syndrome and dermatopathia pigmentosa reticularis, which are both forms of ectodermal dysplasia, also have no fingerprints.
- Gaydos had an abusive family, and suffers from ectodermal dysplasia, which means her skin, hair, nails, teeth and palate didn't develop properly.
- This gene is located in the 13q11 region, which is associated with the genetic diseases Clouston hidrotic ectodermal dysplasia and Kabuki syndrome.
- Research of the disease is ongoing, as only a fraction of the mutations involved with an ectodermal dysplasia subtype have been identified.
- It sometimes occurs on one side in children with the Poland sequence and on both sides in certain types of ectodermal dysplasia.
- Berryman was born with hypohidrotic ectodermal dysplasia which is a rare condition leaving him with no sweat glands, hair, fingernails or teeth.
- Hypohidrotic ectodermal dysplasia is associated with distinctive facial features including a prominent forehead, thick lips, and a flattened bridge of the nose.
- Ectodermal dysplasias can occur in any race but are much more prevalent in caucasians than any other group and especially in fair caucasians.
- This results in air escapement between the folds and the production of breathy voice, which often accompanies the skin abnormalities of ectodermal dysplasia.
- The features ectrodactyly, ectodermal dysplasia and cleft palate have been described with Rudiger syndrome, giving it the rarely used designation " EEC syndrome ".
- The term PPS has also been used for two rare autosomal recessively inherited conditions : " Lethal PPS " and " PPS with Ectodermal Dysplasia ".
- The hypohydrotic symptoms of ectodermal dysplasia described above are evidenced not only in the skin of affected individuals, but also in their phonation and voice production.
- Dental abnormalities in a 5-year-old girl from north Sweden family who suffered from various symptoms of autosomal dominant hypohidrotic ectodermal dysplasia ( HED ) a ) Intraoral view.
- Pachyonychia congenita type 2, an autosomal dominant inherited disorder, is characterized by hypertrophic nail dystrophy, focal keratoderma, multiple pilosebaceous cysts, and a variety of conditions associated with ectodermal dysplasia.
- He has a condition called hypohidrotic ectodermal dysplasia, which causes problems in structures that develop from the ectoderm _ the outer layer of cells that forms in a embryo.
- Ectodermal dysplasia is a rare but severe condition where the tissue groups ( specifically teeth, skin, hair, nails and sweat glands ) derived from the ectoderm undergo abnormal development.
- This gene was identified by its association with ectodermal dysplasia, and specifically with hypohidrotic ectodermal dysplasia, a genetic disorder characterized by defective development of hair, teeth, and eccrine sweat glands.
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