Autosomal Recessive Hypohidrotic Ectodermal Dysplasia

Mapping Intimacies ◽

10.32388/5h9g26 ◽

2020 ◽

Author(s):

Keyword(s):

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Hypohidrotic Ectodermal Dysplasia

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Whole-exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar hyperkeratosis

British Journal of Dermatology ◽

10.1111/bjd.12151 ◽

2013 ◽

Vol 168 (6) ◽

pp. 1353-1356 ◽

Author(s):

A. Haghighi ◽

P. Nikuei ◽

H. Haghighi-Kakhki ◽

N. Saleh-Gohari ◽

S. Baghestani ◽

...

Keyword(s):

Exome Sequencing ◽

Missense Mutation ◽

Whole Exome Sequencing ◽

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Hypohidrotic Ectodermal Dysplasia ◽

Whole Exome ◽

Palmoplantar Hyperkeratosis

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Autosomal recessive hypohidrotic ectodermal dysplasia: Dental manifestations

Oral Surgery Oral Medicine Oral Pathology ◽

10.1016/0030-4220(72)90441-0 ◽

1972 ◽

Vol 33 (5) ◽

pp. 736-742 ◽

Author(s):

Richard C. Bartlett ◽

Lewis R. Eversole ◽

Robert S. Adkins

Keyword(s):

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Hypohidrotic Ectodermal Dysplasia

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Definitive Evidence for an Autosomal Recessive Form of Hypohidrotic Ectodermal Dysplasia Clinically Indistinguishable rom the More Common X-Linked Disorde

The American Journal of Human Genetics ◽

10.1086/513905 ◽

1997 ◽

Vol 61 (1) ◽

pp. 94-100 ◽

Author(s):

R. Munoz ◽

G. Lestringant ◽

V. Sybert ◽

M. Frydman ◽

A. Alswaini ◽

...

Keyword(s):

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Hypohidrotic Ectodermal Dysplasia ◽

Definitive Evidence ◽

Autosomal Recessive Form ◽

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A compound heterozygous mutation in the EDAR gene in a Spanish family with autosomal recessive hypohidrotic ectodermal dysplasia

Archives of Dermatological Research ◽

10.1007/s00403-009-1013-z ◽

2009 ◽

Vol 302 (4) ◽

pp. 307-310 ◽

Author(s):

M. R. Moya-Quiles ◽

M. J. Ballesta-Martínez ◽

V. López-González ◽

G. Glover ◽

E. Guillén-Navarro

Keyword(s):

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Compound Heterozygous Mutation ◽

Heterozygous Mutation ◽

Compound Heterozygous ◽

Hypohidrotic Ectodermal Dysplasia ◽

Spanish Family ◽

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A Novel Splice Site Mutation in theEDARGene Underlies Autosomal Recessive Hypohidrotic Ectodermal Dysplasia in a Pakistani Family

Pediatric Dermatology ◽

10.1111/j.1525-1470.2009.01062.x ◽

2010 ◽

Vol 27 (1) ◽

pp. 106-108 ◽

Author(s):

NAVEED WASIF ◽

MUHAMMAD TARIQ ◽

GHAZANFAR ALI ◽

MUHAMMAD JAWAD HASSAN ◽

WASIM AHMAD

Keyword(s):

Splice Site ◽

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Splice Site Mutation ◽

Pakistani Family ◽

Hypohidrotic Ectodermal Dysplasia ◽

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Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia

Archives of Dermatological Research ◽

10.1007/s00403-009-0975-1 ◽

2009 ◽

Vol 301 (8) ◽

pp. 625-629 ◽

Author(s):

Zahid Azeem ◽

Syed Kamran-Ul-Hassan Naqvi ◽

Muhammad Ansar ◽

Abdul Wali ◽

Abdul Khaliq Naveed ◽

...

Keyword(s):

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Hypohidrotic Ectodermal Dysplasia ◽

Recurrent Mutations

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Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia

Australasian Journal of Dermatology ◽

10.1111/j.1440-0960.2010.00685.x ◽

2010 ◽

Vol 52 (1) ◽

pp. 37-42 ◽

Author(s):

Nosheen Bibi ◽

Saeed Ahmad ◽

Wasim Ahmad ◽

Muhammad Naeem

Keyword(s):

Genetic Analysis ◽

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Molecular Genetic ◽

Molecular Genetic Analysis ◽

Hypohidrotic Ectodermal Dysplasia ◽

Pakistani Families

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AUTOSOMAL RECESSIVE INHERITANCE OF HYPOHIDROTIC ECTODERMAL DYSPLASIA

Pediatric Dermatology ◽

10.1111/j.1525-1470.1990.tb00291.x ◽

1990 ◽

Vol 7 (3) ◽

pp. 242-242 ◽

Author(s):

PÉTER KISS ◽

ÉVA TÖRÖK

Keyword(s):

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Autosomal Recessive Inheritance ◽

Recessive Inheritance ◽

Hypohidrotic Ectodermal Dysplasia

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A novelEDARADD5′-splice site mutation resulting in activation of two alternate cryptic 5′-splice sites causes autosomal recessive Hypohidrotic Ectodermal Dysplasia

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.37607 ◽

2016 ◽

Vol 170 (6) ◽

pp. 1639-1641 ◽

Author(s):

Ajay K. Chaudhary ◽

Katta M. Girisha ◽

Murali D. Bashyam

Keyword(s):

Splice Site ◽

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Splice Site Mutation ◽

Splice Sites ◽

Hypohidrotic Ectodermal Dysplasia ◽

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Hypohidrotic Ectodermal Dysplasia: Argument Against an Autosomal Recessive Form Clinically Indistinguishable from X-Linked Hypohidrotic Ectodermal Dysplasia (Christ-Siemens-Touraine Syndrome)

Pediatric Dermatology ◽

10.1111/j.1525-1470.1989.tb01002.x ◽

1989 ◽

Vol 6 (2) ◽

pp. 76-81 ◽

Author(s):

Virginia P. Sybert

Keyword(s):

Autosomal Recessive ◽

Ectodermal Dysplasia ◽

Hypohidrotic Ectodermal Dysplasia ◽

Autosomal Recessive Form ◽

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