Werner Syndrome

Werner Syndrome Causes, Symptoms and Treatment and Related Disorders ...

Werner Syndrome
National Organization for Rare Disorders, Inc.
Synonyms ...

What is Werner syndrome?
Werner syndrome is characterized by the dramatic, rapid appearance of features associated with normal aging. Individuals with this disorder typically grow and develop normally until they reach puberty.

Werner syndrome
medical dictionary
Cataract in connection with scleroderma, rare; unknown aetiology, M = F, premature aging, short stature, thin, atrophic extremities, generalised osteoporosis, ...

Werner Syndrome: Werner Syndrome patients develop, as young adults, many of the changes associated with aging.

Werner syndrome
Like Bloom syndrome, Werner syndrome is characterized by spontaneous chromosomal instability, resulting in increased susceptibility to cancer and premature aging.

How is Werner syndrome inherited?
Normally, every cell has two copies of each gene: one inherited from the mother and one inherited from the father.

Werner syndrome, NTB (CFSAN), Diphosphonate, Dichloromethylene, DNA Polymerase N3, Double Stranded RNA-Dependent eIF-2 alpha Protein Kinase, East Indies, Enzyme, Disulfide Interchange, Etodolic Acid, Exophiala, Experimental Radiation Injuries, HS-592, ...

Werner syndrome.
Basal cell nevus syndrome.
Other risk factors for soft tissue sarcoma include past treatment with radiation therapy during childhood or for the following types of cancer: ...

Werner syndrome ... reduced hormone production by ovaries
WHIM syndrome ... cervical chronic papillovirus infections
Willebrand disease, acquired ... Menorrhagia
William's syndrome associated Celiac Disease ... Missed menstrual periods ...

von Recklinghausen disease (neurofibromatosis).
Gardner syndrome.
Werner syndrome.
Tuberous sclerosis.
Basal cell nevus syndrome.
Li-Fraumeni syndrome (p53 mutations).

Research indicates that a chemical (hyaluronic acid) may be found in greatly elevated levels in the urine of Hutchinson-Gilford Progeria Syndrome patients. The same abnormality has been found in Werner Syndrome, ...

retinoblastoma
neurofibromatosis type 1 (von Recklinghausen disease or NF1)
tuberous sclerosis
familial adenomatous polyposis (FAP)
Li-Fraumeni syndrome
Werner syndrome
basal cell nevus syndrome ...

In Wiedemann-Rautenstrauch syndrome, also known as neonatal progeroid syndrome, onset of aging begins in the womb, and signs and symptoms are apparent at birth. Werner syndrome begins in adolescence or early adulthood.

girdle muscular dystrophy type 1B, dilated cardiomyopathy, familial partial lipodystrophy, Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia, childhood progeria syndrome (Hutchinson-Gilford syndrome) and a subset of Werner syndrome.

See also: Cancer, Aging, Sclerosis, Symptom, Surgery