Zlotogora-Ogur syndrome

Known as: Ectodermal dysplasia Margarita island type, Ectodermal Dysplasia, Type 4, Bustos Simosa Pinto Cisternas syndrome 
A very rare genetic disorder characterized by cleft lip and palate, sparse scalp hair, and partial syndactyly of the fingers and toes.

Topic mentions per year

Topic mentions per year

1957-2018
0519572017

Papers overview

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2010
2010
Ectodermal dysplasias form a large disease family with more than 200 members. The combination of hair and tooth abnormalities… (More)
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2010
2010
The primary ring, a horseshoe-shaped structure situated between the left and right ventricle and connected superiorly to the… (More)
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2008
2008
Mycoplasma pneumoniae is a bacterial pathogen of the human respiratory tract that causes a wide range of airway diseases as well… (More)
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2006
2006
Poliovirus Receptor Like-1 (PVRL1) is a member of the immunoglobulin super family that acts in the initiation and maintenance of… (More)
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2004
2004
The herpesvirus entry mediator A (HVEM/HveA) and nectin-1 (HveC/CD111) are two major receptors for herpes simplex virus (HSV… (More)
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Highly Cited
2001
Highly Cited
2001
Hay-Wells syndrome, also known as ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome (OMIM 106260), is a rare autosomal… (More)
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Highly Cited
2001
Highly Cited
2001
Non-syndromic cleft lip with or without cleft palate (CL/P, MIM 119530) is among the most common of major birth defects… (More)
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Highly Cited
2000
Highly Cited
2000
Cleft lip, with or without cleft palate (CL/P), is one of the most common birth defects, occurring in 0.4 to 2.0 per 1,000… (More)
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Highly Cited
1999
Highly Cited
1999
Morris (J. Anat., 1976;121:47-64) proposed that the subepicardial mesenchyme might represent a continuing source of… (More)
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1989
1989
A set of three monoclonal antibodies (MoAbs), ED1, ED2, and ED3, has been shown to recognize in situ different subsets of… (More)
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