| 000 | 02844cam a2200325 4500500 | ||
|---|---|---|---|
| 005 | 20250121154623.0 | ||
| 041 | _afre | ||
| 042 | _adc | ||
| 100 | 1 | 0 |
_aKhan, Sher Alam _eauthor |
| 700 | 1 | 0 |
_a Rukan, Ayesha _eauthor |
| 700 | 1 | 0 |
_a Ullah, Asmat _eauthor |
| 700 | 1 | 0 |
_a Bibi, Nousheen _eauthor |
| 700 | 1 | 0 |
_a Humayun, Muhammad _eauthor |
| 700 | 1 | 0 |
_a Ullah, Wasim _eauthor |
| 700 | 1 | 0 |
_a Raza, Rubab _eauthor |
| 700 | 1 | 0 |
_a Muhammad, Noor _eauthor |
| 700 | 1 | 0 |
_a Ahmad, Wasim _eauthor |
| 700 | 1 | 0 |
_a Khan, Saadullah _eauthor |
| 245 | 0 | 0 | _aHomozygous variants of EDAR underlying hypohidrotic ectodermal dysplasia in three consanguineous families |
| 260 | _c2020. | ||
| 500 | _a90 | ||
| 520 | _aBackground: Hypohidrotic ectodermal dysplasia (HED) is a congenital anomaly characterized by hypohydrosis, hypotrichosis and hypodontia. Mutations in at least four genes (EDAR, EDARADD, WNT10A, TRAF6) have been reported to cause both autosomal recessive and autosomal dominant forms of HED. Mutations in two other genes (EDA and IKBKG) have been reported to cause X-linked HED. Objectives: To clinically characterize three consanguineous families (A-C) segregating with autosomal recessive HED and identify possible disease-causing variants of EDAR and EDARADD genes. Materials and Methods: The genes, EDAR and EDARADD, were sequenced in Family A and C, and exome sequencing was performed in Family B. Additionally, in Family A and C, the effect of the identified variants was examined by analysis of EDAR mRNA, extracted from hair follicles from both affected and unaffected members. Results: Sequence analysis revealed three possible disease-causing EDAR variants including a novel splice acceptor site variant (IVS3-1G > A) in Family A and two previously reported mutations (p.[Ala26Val], p.[Arg25*]) in the two other families. Previously, the nonsense variant p.(Arg25*) was reported only in the heterozygous state. Analysis of the RNA, extracted from hair follicles, revealed skipping of a downstream exon in EDAR and complete degradation of EDAR mRNA in affected members in family A and C, respectively. Computational modelling validated the pathogenic effect of the two variants identified in Family B and C. Conclusion: The three variants reported here expand the spectrum of EDAR mutations associated with HED which may further facilitate genetic counselling of families segregating with similar disorders in the Pakistani population. | ||
| 690 | _ahypohidrotic ectodermal dysplasia | ||
| 690 | _aRNA analysis | ||
| 690 | _ahomozygous variants | ||
| 690 | _aprotein modelling | ||
| 690 | _aEDAR | ||
| 786 | 0 | _nEuropean Journal of Dermatology | 30 | 4 | 2020-07-01 | p. 408-416 | 1167-1122 | |
| 856 | 4 | 1 | _uhttps://shs.cairn.info/revue-european-journal-of-dermatology-2020-4-page-408?lang=fr&redirect-ssocas=7080 |
| 999 |
_c602813 _d602814 |
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