Wiedemann-Rautenstrauch syndrome
WRS

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Prevalence (%) of clinical parameters based on data from 1 references describing 18 individuals







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Pubmed id number as a reference Organ system affected
Number of patients in the reference Percent affected patients (Between 0 and 1, eg. 0.1 = 10%)
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List of symptoms



Symptom/sign Organ system Percent affected Pubmed id Added on(yyyy-mm-dd) Edit/add reference
Intrauterine growth retardation multi 100 % 28447407 2022-01-07
Short stature skeletal 100 % 28447407 2022-01-07
Alopecia integumentary 100 % 28447407 2022-01-07
Thin lips multi 100 % 28447407 2022-01-07
Decreased subcutaneous fat integumentary 100 % 28447407 2022-01-07
Wide anterior fontanel skeletal 94 % 28447407 2022-01-07
Triangular face skeletal 94 % 28447407 2022-01-07
Deep-set eyes skeletal 89 % 28447407 2022-01-07
Small mouth integumentary 89 % 28447407 2022-01-07
Downturned corners of mouth multi 89 % 28447407 2022-01-07
Localized fat accumulation integumentary 71 % 28447407 2022-01-07
Hypertriglyceridemia circulatory 60 % 28447407 2022-01-07
Hypertonia nervous 56 % 28447407 2022-01-07
Acanthosis nigricans integumentary 53 % 28447407 2022-01-07
Broad eyebrows integumentary 39 % 28447407 2022-01-07
Convex nasal bridge skeletal 39 % 28447407 2022-01-07
Hypodontia skeletal 39 % 28447407 2022-01-07
Small ears integumentary 33 % 28447407 2022-01-07
Ataxia nervous 25 % 28447407 2022-01-07
Osteoporosis skeletal 19 % 28447407 2022-01-07
Tremor nervous 19 % 28447407 2022-01-07
Hypomyelination nervous 14 % 28447407 2022-01-07
Seizures nervous 13 % 28447407 2022-01-07
Diabetes mellitus endocrine 11 % 28447407 2022-01-07



List of references:


Wiedemann-Rautenstrauch syndrome: A phenotype analysis.
Stefano Paolacci, Debora Bertola, José Franco, Shehla Mohammed, Marco Tartaglia, Bernd Wollnik, Raoul C Hennekam,



American journal of medical genetics. Part A - Jul 2017