Marden–Walker syndrome

Marden-Walker syndrome
Synonyms	Connective tissue disorder Marden Walker type
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Marden–Walker syndrome (MWS) is a rare autosomal recessive congenital disorder.<ref name=omim>Online Mendelian Inheritance in Man (OMIM) 248700 </ref><ref name=mwsar>,

 Renal anomalies in Marden-Walker syndrome: A clue for prenatal diagnosis, 
 American Journal of Medical Genetics, 
 
 Vol. 57(Issue: 3),
 pp. 417–419,
 DOI: 10.1002/ajmg.1320570310,
 PMID: 7677143,</ref> It is characterized by blepharophimosis, microcephaly, micrognathia, multiple joint contractures, arachnodactyly, camptodactyly, kyphoscoliosis and delayed motor development and is often associated with cystic dysplastic kidneys, dextrocardia, Dandy–Walker malformation and agenesis of corpus callosum.<ref name="badano2006">, 
 The ciliopathies: an emerging class of human genetic disorders, 
 Annu Rev Genom Hum Genet, 
 2006,
 Vol. 7,
 pp. 125–148,
 DOI: 10.1146/annurev.genom.7.080505.115610,
 PMID: 16722803,</ref>

Signs and symptoms

Most of the signs of MWS are present during the neonatal period. The most common signs at this state are multiple congenital joint contractures, dysmorphic features with mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high arched palate, low-set ears, arachnodactyly, chest deformation as pectus, kyphoscoliosis and absent deep tendon reflexes are frequent minor malformations have also been described and consist of renal anomalies, cardiovascular abnormalities, hypospadias, omphalomesenteric duct, hypertriphic pyloric stenosis, duodenal bands, hyoplasticTemplate:Typo help inline right lower lobe of the lung, displacement of the larynx to the right and vertebral abnormalities, cerebral malformations.<ref>

Marden-Walker syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program(link). {{{website}}}.

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• 75% of children with MWS have blepharophimosis, small mouth, micrognathia, kyphosis/scoliosis, radio ulnar synostose and multiple contractures.
• They have severe developmental delay; congenital joint contractures and blepharophimosis should be present in every patient
• 2 out of 3 of the following signs should be manifested: post natal growth, mask-like faces, retardation, and decreased muscular mass.
• Some may require additional signs such as; micrognathia, high arched or cleft palate, low set ears, kyphoscoliosis.
• The symptoms of MWS are normally diagnosed during the newborn period

Progression

The natural history of MWS is not well known: many patients died in infancy and clinical follow-up has been reported in few surviving adults. However, diagnosis may be more difficult to establish in adults patients, such as: blepharophimosis, contractures, growth retardation, and developmental delay, whereas minor face anomalies are less noticeable as the patient grows older.<ref>https://www.orpha.net/data/patho/GB/uk-MardenWalker.pdf</ref> Throughout the development of the patient from young child to older adult changes the behavior drastically, from kindness to restless and hyperactive to aggressive. ^{(June 2020)}

Cause

MWS is a heterogeneous, initially described as a syndrome. But this condition is more on the lines of a phenotypic expression of various heterogeneous diseases and belongs to the second group in the classification of arthrogryposis. Unknown congenital myopathy has been suspected to underlie MWS due to muscular involvement, but extension of the neuromuscular systems failed to identify a primary myopathy in patients with MWS. Secondary muscle involvement from a CNS lesion may occur. This could lead to congenital weakness with hypoatonia deep tendon reflex.<ref>

Marden Walker Syndrome(link). {{{website}}}.

</ref>

Genetics

MWS is inherited in an autosomal recessive manner.<ref name=mwsar/> This means the defective gene responsible for the disorder is located on an autosome, and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but usually do not experience any signs or symptoms of the disorder.

Pathophysiology

Though the pathomechanism of Marden–Walker syndrome is unknown, it may be caused by a genetic defect which manifests as a dysfunctional molecular mechanism in the primary cilia structures of the cell. These organelles are present in many cellular types throughout the human body. The cilia defects adversely affect "numerous critical developmental signaling pathways" essential to cellular development.<ref name="badano2006"/>

Diagnosis

Marden-Walker syndrome (MWS) is diagnosed based on a clinical history, exam, and additional medical tests, such as imaging and nerve conduction studies. In addition, several other conditions resemble Marden-Walker syndrome and may need to be excluded.

Management

The only treatment for MWS is only symptomatic, with multidisciplinary management<ref>http://www.rightdiagnosis.com/m/marden_walker_syndrome/intro.htm</ref> Specialists who may be involved in the care of someone with Marden-Walker syndrome include:

• Medical geneticist
• Neurologist
• Orthopedist
• Physical therapist
• Occupational therapist

Epidemiology

There have been 30 cases of Marden-Walker Syndrome reported since 1966.Template:Where The first case of this was in 1966 a female infant was diagnosed with blepharophimosis, joint contractures, arachnodactyly and growth development delay. She ended up passing at 3 months due to pneumonia. ^{(July 2013)}

External links

• Marden-Walker syndrome at NIH's Office of Rare Diseases

• Marden Walker like syndrome at NIH's Office of Rare Diseases

Online Mendelian Inheritance in Man (OMIM) 600920