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Denys-Drash Syndrome

Known as: Denys Drash Syndrome, Syndrome, Drash, Drash Syndrome 
A rare disorder that causes kidney failure before age 3, abnormal development of the sexual organs, and, in most cases, Wilms tumor (a type of kidney… 
National Institutes of Health

Related topics

Related topics

26 relations
Ambiguous GenitaliaAutosomal dominant inheritanceChromosomes, Human, Pair 11Denys-Drash Syndrome, Incomplete

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
WARM MOLECULAR GAS IN LUMINOUS INFRARED GALAXIES
We present our initial results on the CO rotational spectral line energy distribution (SLED) of the J to J−1 transitions from J… 
2013
2013
A familial WT1 mutation associated with incomplete Denys–Drash syndrome
Denys–Drash syndrome (DDS) is a rare disorder characterized by nephropathy, male pseudohermaphroditism, and wilms tumor. Cases… 
Review
2005
Review
2005
Congenital diaphragmatic hernia in WAGR syndrome
Wilms tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene deletion syndrome… 
2004
2004
The Periegesis of Dionysius and the traditions of hellenistic poetry
Cette étude examine certaines des manières utilisées par Denys pour exploiter la poésie du IIIe s. av. J.-C. Pour Denys le plus… 
2003
2003
Bridging the Gap Between Underspecification Formalisms: Minimal Recursion Semantics as Dominance Constraints
Minimal Recursion Semantics (MRS) is the standard formalism used in large-scale HPSG grammars to model underspecified semantics… 
2003
2003
WT1 gene mutation responsible for male sex reversal and renal failure: the Frasier syndrome.
Review
2002
Review
2002
A review of the phenotypic variation due to the Denys‐Drash syndrome‐associated germline WT1 mutation R362X
The gene WT1 is required for the normal development and function of the urogenital tract. Constitutional mutations are associated… 
1996
1996
Genotype/phenotype correlations in Wilms' tumor.
Study of genotype/phenotype relationships involving the Wilms' tumor (WT) gene, WT1, in WT patients has provided insights into… 
1994
1994
WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin
Denys-Drash syndrome (DDS) is characterized by early onset nephropathy, pseudohermaphroditism in males and a high risk for… 
1959
1959
THE CONTRIBUTION OF OBSTETRICAL FACTORS TO SERIOUS PHYSICAL AND MENTAL HANDICAP IN CHILDREN
THE hazards of maternity which may cause death or damage to the child may be roughly divided into two groups: (a) abnormal… 
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