Geroderma osteodysplasticum
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Prevalence (%) of clinical parameters based on data from 3 references describing 11 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
Hip dysplasia skeletal 100 % 474638 2022-11-17
Vertebral anomalies skeletal 100 % 474638 2022-11-17
Scoliosis skeletal 100 % 474638 2022-11-17
Pseudoepiphyses skeletal 100 % 474638 2022-11-17
Pes planus skeletal 100 % 474638 2022-11-17
Protruding abdomen skeletal 100 % 474638 2022-11-17
Dental malocclusion skeletal 100 % 474638 2022-11-17
Skin wrinkles integumentary 100 % 474638 2022-11-17
Skin wrinkles integumentary 100 % 9018419 2022-11-17
Decreased skin turgor integumentary 100 % 631850 2022-11-17
Osteoporosis skeletal 100 % 631850 2022-11-17
Ear malformation integumentary 100 % 9018419 2022-11-17
Joint dislocation skeletal 100 % 9018419 2022-11-17



List of references:


Gerodermia osteodysplastica hereditaria: report of three affected brothers and literature review.
R Lisker, A Hernández, M Martínez-Lavin, O Mutchinick, C Armas, P Reyes, J Robles-Gil,



American journal of medical genetics - 1979



Gerodermia osteodysplastica in a Bedouin sibship: further delineation of the syndrome.
N A al-Torki, S A al-Awadi, L Cindro-Heberie, M A Sabry,



Clinical dysmorphology - Jan 1997



Geroderma osteodysplastica. A report of two affected families.
A G Hunter, J T Martsolf, C G Baker, M H Reed,



Human genetics - Feb 1978