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Visceromegaly

Abnormal increased size of the viscera of the abdomen. [HPO:probinson]
National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

Hypertrophic disorder of skin, unspecifiedHypertrophy
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Pearls & Oy-sters: Niemann-Pick disease type C in a 65-year-old patient
A 65-year-old, right-handed man of Polish ancestry developed insidious onset, gradually progressive gait ataxia at the age of 55… 
2003
2003
Schwannoma of ileocecal valve: an incidental finding in a patient with rectal carcinoma
2001
2001
Cataracte congénitale et syndrome de Wiedemann-Beckwith
Le syndrome de Wiedemann-Beckwith est un syndrome polymalformatif congenital qui associe plusieurs anomalies : omphalocele… 
1999
1999
Síndrome de Wiedemann-Beckwith: Análisis clínico-epidemiológico de una serie consecutiva de casos en España
La frecuencia minima del sindrome estimada en Espana es de 0, 13 por 10000 recien nacidos vivos. Los ninos pesan mas para su edad… 
1981
1981
Morphological diagnosis of Niemann-Pick disease type C by skin and conjunctival biopsies.
Skin and conjunctival biopsies were performed in six children with mental deterioration, incoordination, involuntary movements… 
1974
1974
Small bowel dilatation in Ehlers-Danlos syndrome--an unreported gastrointestinal manifestation.
Ehlers-Danlos syndrome is an interesting hereditary disease which involves the collagen fibres of connective tissue presumably at… 
1972
1972
Exomphalos-macroglossia-gigantism (visceromegaly) syndrome. (The Beckwith-Wiedemann syndrome).
The 4 most characteristic clinical abnormalities of the Beckwith-Wiedemann syndrome are omphalocele or umbilical hernia… 
1971
1971
The Beckwith-Wiedemann syndrome. Seven new cases.
Seven cases of the Beckwith-Wiedemann syndrome are reported. The features of the syndrome may include macroglossia, omphalocele… 
1971
1971
Hereditary essential myoclonus.
Review
1971
Review
1971
Macroglossia, omphalocele, visceromegaly, cytomegaly of the adrenal cortex and neonatal hypoglycemia.