BIOMAT Database Logo BIOMAT Database Logo

[Hereditary chronic pancreatitis: an autosomal dominant disease (author's transl)]. 1979

C Stoll, and R Bigel, and J M Levy

We have studied a family in which three people, two child and an adult had hereditary pancreatitis. Hereditary pancreatitis is not a common disease. Abdominal pain is usually the first clinical sign in children. The knowledge of the existence of such a disease and familiarity with the family history of the child allow the pediatrician to make the diagnosis as soon as the first crisis appears. Surgery is thus avoided. Our studies show definitively that this disease is hereditary and is autosomal dominant with a strong decrease of the penetrance.

UI MeSH Term Description Entries
D008297 Male Males
D010195 Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. Acute Edematous Pancreatitis,Acute Pancreatitis,Pancreatic Parenchyma with Edema,Pancreatic Parenchymal Edema,Pancreatitis, Acute,Pancreatitis, Acute Edematous,Peripancreatic Fat Necrosis,Acute Edematous Pancreatitides,Acute Pancreatitides,Edema, Pancreatic Parenchymal,Edematous Pancreatitides, Acute,Edematous Pancreatitis, Acute,Fat Necrosis, Peripancreatic,Necrosis, Peripancreatic Fat,Pancreatic Parenchymal Edemas,Pancreatitides, Acute,Pancreatitides, Acute Edematous,Parenchymal Edema, Pancreatic,Peripancreatic Fat Necroses
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D002908 Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). Chronic Condition,Chronic Illness,Chronically Ill,Chronic Conditions,Chronic Diseases,Chronic Illnesses,Condition, Chronic,Disease, Chronic,Illness, Chronic
D005260 Female Females
D005799 Genes, Dominant Genes that influence the PHENOTYPE both in the homozygous and the heterozygous state. Conditions, Dominant Genetic,Dominant Genetic Conditions,Genetic Conditions, Dominant,Condition, Dominant Genetic,Dominant Gene,Dominant Genes,Dominant Genetic Condition,Gene, Dominant,Genetic Condition, Dominant
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

C Stoll, and R Bigel, and J M Levy
[Syndrome of symphalangism and stapes fixation: an autosomal dominant hereditary disease (author's transl)].
October 1978, Deutsche medizinische Wochenschrift (1946),
C Stoll, and R Bigel, and J M Levy
[Hereditary microcephaly with autosomal dominant chorioretinal dysplasia (author's transl)].
January 1981, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris,
C Stoll, and R Bigel, and J M Levy
[Color vision in autosomal dominant hereditary optic atrophy (author's transl)].
September 1975, Nippon Ganka Gakkai zasshi,
C Stoll, and R Bigel, and J M Levy
[Secundum atrial septal defect with prolonged atrioventricular conduction: an autosomal dominant hereditary cardiac defect (author's transl)].
October 1977, Deutsche medizinische Wochenschrift (1946),
C Stoll, and R Bigel, and J M Levy
[Osteomesopycnosis. A new autosomal dominant osteosclerosing bone disease (author's transl)].
March 1980, Archives francaises de pediatrie,
C Stoll, and R Bigel, and J M Levy
[Autosomal dominant hereditary polycystic kidney disease].
August 1995, Casopis lekaru ceskych,
C Stoll, and R Bigel, and J M Levy
[Centronuclear myopathy with autosomal dominant inheritance(author's transl)].
January 1975, Humangenetik,
C Stoll, and R Bigel, and J M Levy
[Ectrodactyly, ectodermal dysplasia, and cleft lip and palate: an hereditary syndrome with an autosomal dominant mode of inheritance (author's transl)].
October 1973, Zeitschrift fur Kinderheilkunde,
C Stoll, and R Bigel, and J M Levy
[Hereditary pancreatitis in early childhood (author's transl)].
December 1980, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde,
C Stoll, and R Bigel, and J M Levy
Haemosuccus pancreaticus associated with autosomal dominant polycystic kidney disease and chronic pancreatitis.
August 2023, BMJ case reports,
Copied contents to your clipboard!