Minerva Med. 1983 Feb 25;74(7):301-6.

[Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree].

[Article in Italian]

De Marchi S, Proto G, Jengo A, Collinassi P, Basile A.

Abstract

Assessment of the pedigree of 7 persons in 3 generations showed that interpretation of the transmission modality of renal glycosuria may be influenced by the diagnostic criteria employed. Analysis of renal glucose curves and evaluation of glycosuria after an oral glucose tolerance test made it clear that albeit slight detects could be detected in family members who would be regarded as healthy according to the criteria of Marble. Distribution of the character pointed to dominant transmission, as opposed to the recessive autosomal transmission favoured in the literature. Variations in the clinical gravity of the tubular defect may be ascribable to a difference in the expressiveness of the abnormal gene or to genetic heterogeneity. Persons homozygous and heterozygous for the gene were present in the pedigree concerned.

PMID:: 6828258; [PubMed - indexed for MEDLINE]

Publication Types, MeSH Terms

Publication Types

MeSH Terms

Supplemental Content

Save items

Related citations in PubMed

Renal glycosuria (a family study). [J Indian Med Assoc. 1984]
Renal glycosuria (a family study).
Dash R, Mishra K, Das PC, Das RK 3rd, Mohakur AC, Padhi PK, Mishra D. J Indian Med Assoc. 1984 Aug; 82(8):287-9.
Autosomal dominant inheritance of retinoschisis. [Am J Ophthalmol. 1982]
Autosomal dominant inheritance of retinoschisis.
Yassur Y, Nissenkorn I, Ben-Sira I, Kaffe S, Goodman RM. Am J Ophthalmol. 1982 Sep; 94(3):338-43.
Autosomal recessive inheritance of renal glycosuria. [Metabolism. 1971]
Autosomal recessive inheritance of renal glycosuria.
Elsas LJ, Busse D, Rosenberg LE. Metabolism. 1971 Oct; 20(10):968-75.
Review Historical evidence for the genetic heterogeneity of pseudoxanthoma elasticum. [Br J Dermatol. 1975]
Review Historical evidence for the genetic heterogeneity of pseudoxanthoma elasticum.
Pope FM. Br J Dermatol. 1975 May; 92(5):493-509.
Review Autosomal dominant cornea plana: clinical findings in a Cuban family and a review of the literature. [Ophthalmic Genet. 1997]
Review Autosomal dominant cornea plana: clinical findings in a Cuban family and a review of the literature.
Sigler-Villanueva A, Tahvanainen E, Lindh S, Dieguez-Lucena J, Forsius H. Ophthalmic Genet. 1997 Jun; 18(2):55-62.

See reviews... See all...

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Compound
PubChem chemical compound records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records. Multiple substance records may contribute to the PubChem compound record.
Gene (OMIM)
Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide (Weighted)
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
OMIM (calculated)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as references in the light bulb links within or in the citations at the end of the OMIM record. The references available through the light bulb link are collected using the PubMed related articles algorithm to identify records with similar terminology to the OMIM record.
OMIM (cited)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein (Weighted)
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.
Substance
PubChem chemical substance records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records.

Recent activity

Clear Turn Off Turn On

[Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary tr...
[Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree].
Minerva Med. 1983 Feb 25 ;74(7):301-6.

PubMed
[Clinic and therapy of anal fissure (author's transl)].
[Clinic and therapy of anal fissure (author's transl)].
Leber Magen Darm. 1978 Aug ;8(4):218-20.

PubMed
Control of timing of cell cycle events in fission yeast by the wee 1+ gene.
Control of timing of cell cycle events in fission yeast by the wee 1+ gene.
Nature. 1983 Mar 10 ;302(5904):153-5.

PubMed
Ménière's disease in children.
Ménière's disease in children.
Laryngoscope. 1978 Sep ;88(9 Pt 1):1504-11.

PubMed
Fetal alcohol syndrome. A great paediatric imitator.
Fetal alcohol syndrome. A great paediatric imitator.
Med J Aust. 1983 Mar 19 ;1(6):266-9.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to:

[Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree].

Abstract

Publication Types, MeSH Terms

Publication Types

MeSH Terms

Supplemental Content

Save items

Related citations in PubMed

Related information

Recent activity

Simple NCBI Directory

Getting Started

Resources

Popular

Featured

NCBI Information