IthaMaps

Welcome to IthaMaps

IthaMaps is a global epidemiology database of heamoglobinopathies, illustrating published data on a dynamic global to regional map. Country-specific information on haemoglobinopathy-related policies, prevalence, incidence and overall disease burden is given, including relative allele frequencies of specific globin mutations in each country and/or region, dynamically linked to corresponding IthaGenes entries.

IthaMaps content was supported by partnership with the HVP Global Globin 2020 Challenge

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General information for Mauritania

Mauritania

Continent:	Africa
Capital:	Nouakchott
Population:	3205060
Area (in sq km):	1030700.0

Haemoglobinopathy-specific healthcare policy information for Mauritania

Healthcare policy		Comment/Info	Reference
SCD newborn screening:	No
Rare disease patient registry:	No	http://africa-rare.org/

Prevalence and incidence of major haemoglobinopathies in Mauritania

Haemoglobinopathy		Comment/Info	Reference
Prevalence of β-thalassaemia carriers:	2.57 % of the population		[PMID: 12107561]
Prevalence of sickle cell disease carriers:	8.71 % of the population		[PMID: 12107561]
Prevalence of Hb C carriers:	3 % of the population		[PMID: 12107561]
Incidence of sickle cell disease:	433 affected births/year	Median value estimated using statistical model and demographic data.	[PMID: 23103089]

Global Burden of Disease data for Mauritania

Migration data for Mauritania

Mutation frequencies in Mauritania

Overview (most frequent mutations with their observed average values and range)

β-locus

CD 24 GGT>GGA [Gly>Gly]: 13.3 %

Detailed mutation frequencies

	Entry ID	Locus	Region	Ethnic Group	Population Type	Sample Size	Study period (from)	Study period (to)	Reference	Comments
	21250	β-locus	Nouakchott	Mauritanian	Carriers	15		2015	26044735	Frequencies are shown for beta-globin gene mutations. Study samples were acquired from the Universite des Sciences de Technologies et de Medicine, Nouakchott. The CD24 GGT>GGA mutation was found in two beta-thal carriers from two different sub-ethnic groups; the Pulhar and the Moors groups, both of Black origin.

Organisations in Mauritania

Organisations in Mauritania are currently not available

Microattributions

A/A	Contributor(s)	Date	Comments
1	Elion, Jacques	2017-10-17	Information on SCD newborn screening reviewed.

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Important Note: The relative allele frequencies presented in IthaMaps are not calculated by ITHANET, but they are extracted from the corresponding publications. ITHANET is not responsible for any mistakes in the data. Please use this information with caution! We encourage scientists that have more detailed or updated epidemiological information to contact us.

Disclaimer: The information on this website is provided as an information resource only and must not to be used as a substitute for professional diagnosis and treatment. The ITHANET Portal and IthaMaps are not responsible or liable for any advice, course of treatment, diagnosis or any other information, services or products that an individual obtains through this website.

Note: The information you provide for the specific country will appear on the IthaMaps website and your contribution will be acknowledged.

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Healthcare Policies

Health-policy	Select one Answer	Comment
Prevention programme
SCD newborn screening
Prenatal screening
Antenatal screening
Haemoglobinopathies patient registry
Rare disease patient registry
Dedicated treatment centres
Blood transfusion availability
Iron chelation availability
MRI facilities
Patient associations
Genetic counselling

Status of major Haemoglobinopathies

In Expected Incidence of β-thalassaemia and sickle cell disease please provide the number of expected affected births/year (without prevention).
In Incidence of β-thalassaemia and sickle cell disease please provide the number of affected births/year (after prevention).

Haemoglobinopathy	Provide value		Comment
Prevalence of β-thalassaemia carriers		% of the population
Prevalence of sickle cell disease carriers		% of the population
Prevalence of α-thalassaemia carriers		% of the population
Prevalence of Hb E carriers		% of the population
Prevalence of Hb C carriers		% of the population
Expected incidence of β-thalassaemia		expected affected births/year
Expected incidence of sickle cell disease		expected affected births/year
Expected incidence of α-thalassaemia		expected affected births/year
Incidence of β-thalassaemia		affected births/year
Incidence of sickle cell disease		affected births/year
Incidence of α-thalassaemia		affected births/year
Known β-thalassaemia patients		patients
Known sickle cell disease patients		patients

Mutation Frequencies

Please provide details about publications reporting mutation frequencies in the country of reference (either country-wide studies or region-specific studies).

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