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Home Page > Diseases by Region: Ashkenazi > Dihydrolipoamide Dehydrogenase Deficiency

Dihydrolipoamide Dehydrogenase Deficiency (DLD)
by Yael Rosenberg, RN

Description
Dihydrolipoamide dehydrogenase deficiency (DLD) also known as Maple Syrup Urine Disease Type 3 is an autosomal recessive disease affecting the body’s ability to breakdown certain amino acids and their byproducts. Located on chromosome 7 the DLD gene is responsible for instructing the cell to produce a protein named dihydrolipoamide dehydrogenase. This specific protein is part of a group of enzymes that work together to breakdown certain molecules that produce energy. The gene mutations change the structure of the E3 component thereby preventing enzymatic breakdown of essential amino acids. The buildup of the amino acids is detrimental to the cells especially those in the nervous system. The mortality rate is high. Onset of symptoms may be in infancy or in adulthood.

Symptoms
In the first few weeks or months of life patients may be free of any symptoms except for incidences of low blood sugar.
As they grow older the infant develops:
   • Progressively worsening neurological issues
   • Diminished muscle tone
   • Dystonia
   • Ataxia
   • Microcephaly
   • Seizures
   • Developmental delay and Mental retardation
   • Failure to thrive
   • Liver enlargement
   • Frequent vomiting and abdominal pain
   • Blindness
   • Coma

Incidence and Carriers
Carrier Frequency: 1 in 96 in individuals of Jewish Ashkenazi decent
Detection rate (for two specific mutations): 95% of carriers in the Ashkenazi Jewish population

In the general population this very rare disease has a prevalence of 1/1,000,000.
 

Treatment
Currently this is no cure or treatment for DLD.

Testing
   • Mutation analysis for DLD
   • Newborn screening
   • Prenatal testing

Laboratories and Screening
The following laboratories offer genetic testing for AAT Deficiency:
   •  United States
   •  Israel
   •  Canada
   •  India
   •  Europe

UNITED STATES
Medical Genetics Laboratories
Baylor College of Medicine
One Baylor Plaza, NAB 2015
Houston, TX 77030
Phone: (800) 411-GENE (4363)
Fax: (713) 798-2787
Email: genetictest@bcm.edu
Client Services Manager
Alejandra Quick
Phone: (713) 798-7656
Fax: (713) 798-2787
Email: ahquick@bcm.edu

Emory University School of Medicine
Emory Molecular Genetics Laboratory
Atlanta, GA
Phone: (404) 778-8500
Fax: (404) 778-8559
Email: eglgc@emory.edu

GeneDx
207 Perry Parkway
Gaithersburg, MD 20877
Phone: (301) 519-2100
Fax: (301) 519-2892

Genzyme Genetics
Molecular Diagnostic Laboratory
3400 Computer Drive
Westborough, MA 01581
Phone: (508) 898-9001
Fax: (508) 389-5549
Toll Free: (800) 255-7357

Genzyme Genetics General Inquiries:
Phone: (800)-357-5744
Fax: (508) 389-5549
Client Services - Reproductive Genetics
Phone: (800) 848-4436

Mount Sinai Genetic Testing Laboratory (DNA Division)
The Mount Sinai Medical Center
One Gustave L. Levy Place
New York, NY 10029-6574
Phone: (212) 241-3055
Fax: (212) 241-9467
Email: rochelle.pakier@mssm.edu

University Hospitals
The Center for Genetics Laboratory
10524 Euclid Avenue, 6th Floor
Cleveland, OH 44106
Phone: (216) 983-1134
Fax: (216) 983-1144
Web: http://www.chglab.com 
 
ISRAEL
GGA –Galil Genetic Analysis Ltd
P.O.B. 3664
Kazerin, Hatzafon, Israel 12900
Phone: (+972) 4-900-7100
Fax: (+972) 4-900-7111
Email: gga@gga.org.il

Pronto Diagnostic Ltd.
19A Habarzel Street
Ramat Hachayal
Tel Aviv, Israel 69710
Phone: (+972) 73-312-6155
Fax: (+972) 73-212-6144
Email: info@prontodiagnostics.com

EUROPE
   •  Spain

SPAIN
Universidad Autonoma de Madrid
Centro de Diagnostico de Enfermedades Moleculares
Madrid, Spain
Director: Magdalena Ugarte, PhD
Genetic Counselor: Dr Lourdes Ruiz Desviat, PhD
Phone: (+34) 911-964-566
Fax: (+34) 914-974-863
Email: lruiz@cbm.uam.es


Support Groups
Maple Syrup Urine Disease Family Support Group
Phone: (740) 548-4475
Email: dbulcher@aol.com

MSUD Family Support Group
24806 SR 119
Goshen, IN 46526
Phone: (219) 862-2992
Fax: (219) 862-2012
Email: msd-support@juno.com 
Web: http://www.msud-support.org

Maple Syrup Urine Disease Family Support Group (MSUDFSG)
1106 Old Line Road
Manheim, PA 17545
Phone: (717) 665-5961

Climb (Children Living with Inherited Metabolic Diseases)
Family Services
Toll free: (+44) (0)800 652 3181 (open 10am – 4pm BST)
Phone: (+44) (0) 845-241-2172
Email: fam.svcs@climb.org.uk

SUGGESTED READING

Jewish Genetic Disorders: A Layman's Guide: Guide to genetic disorders affecting  the Jewish population more than the non-Jewish. Includes basic facts on genetics & genetic disorders.
     ------------
Books: Jewish Genetic Diseases

 

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