coinheritance

(ˌkəʊɪnˈhɛrɪtəns)

joint inheritance

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References in periodicals archive ?

Among these, 99 (34.6%) patients showed AT coinheritance (ATC) (Table 1).

Frequency of Alpha Thalassaemia in homozygous Beta Thalassaemia paediatric patients and its clinical impact at a blood disease centre in Karachi, Pakistan

A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor.

BETA-TALASEMIA: UN MUNDO DE COMPLICACIONES CON NUEVAS ALTERNATIVAS DE TRATAMIENTO

(14,15) Finally, coinheritance of [alpha]-thalassemia and SCD has been associated with a reduced sickled Hb concentration in erythrocytes, leading to reduced Hb S polymerization, lowered sickling and rate of hemolysis.

New variants in beta globin gene among the Palestinian refugees with sickle cell disease in Lebanon

Given SCT status and history of recurrent exercise-induced hematuria and proteinuria, it is likely that coinheritance of p.

Multifactorial Origin of Exertional Rhabdomyolysis, Recurrent Hematuria, and Episodic Pain in a Service Member with Sickle Cell Trait

Harikrishna et al., "Coinheritance of the membrane frizzled-related protein ocular phenotype and glycogen storage disease type Ib," Ophthalmic Genetics, vol.

Nanophthalmos: A Review of the Clinical Spectrum and Genetics

Coinheritance of HFE H63D mutation may enhance the iron overload in patients with BTM, which may necessitate a more intensive iron chelation therapy in these patients to prevent hemosiderosis development.

The Correlation of Cardiac and Hepatic Hemosiderosis as Measured by T2*MRI Technique with Ferritin Levels and Hemochromatosis Gene Mutations in Iranian Patients with Beta Thalassemia Major

The mean of hematological indices among beta-thalassemia and alpha-beta-thalassemia carriers Parameters Mean (1)[+ or -]SD Mean(2)[+ or -]SD Hb (g/dl) 12.4[+ or -]1.8 13.1 [+ or -]2.0 RBC(106/ul) 6.10[+ or -]0.7 6.12[+ or -]0.7 MCV(fl) 63.2[+ or -]5.0 65.4[+ or -]6.1 MCH (pg) 20.3[+ or -]2.0 20.9[+ or -]2.2 HbA2 (%) 5.3[+ or -]0.7 5.2[+ or -]0.7 (1.) The mean values with standard deviations for 100 beta-thai carriers without any common alpha deletion are shown in this column for specific parameters (2.) The mean values with standard deviations for 43 individuals with coinheritance of common alpha deletion and beta-thai mutation are shown in this column for specific parameters

The Frequency and Importance of Common [alpha]-globin Gene Deletions Among [beta]-Thalassemia Carriers in an Iranian Population

showed that coinheritance of alpha thalassemia with homozygous beta thalassemia resulted in melioration of the beta thalassemia.19 Several studies have reported that clinical picture of the disease changed due to the interaction of a-thal deletions with homozygous b-thal mutations.20, 21

Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population

Many of the subjects analyzed in our series [50, 51, 64, 85] showed coinheritance of different genetic alterations in the minor MMR genes (Table 3) we speculate a likely additive role of low penetrance alleles in the disease development, in favor of a putative polygenic inheritance for Lynch syndrome, according to recent literature data [87-89].

Novel Implications in Molecular Diagnosis of Lynch Syndrome

Sickle cell anemia (HbSS/HbS-Beta thalassemia zero) accounts for 70% of cases of sickle cell disease in populations of African ethnicity, with most of the remainder having hemoglobin SC disease (HBSC disease) due to the coinheritance of the [[beta].sup.s] and [[beta].sup.c] alleles [2,3].