Disease #07083 (MSUD1B (maple syrup urine disease, type Ib), OMIM:620698)

Official abbreviation MSUD1B
Name maple syrup urine disease, type Ib
OMIM ID 620698
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene BCKDHB
Associated tissues -
Disease features -
Remarks -
Date created 2024-05-25 09:41:09 +02:00 (CEST)
Date last edited N/A


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00450471 3bINP-013 PubMed: Vela-Amieva 2024 Likely consanguinity M no Mexico Mexican - - - - MSUD1B - BCKDHB BCKDHB 1 1 Miriam Erandi Reyna-Fabián
00451365 3bINP-020 PubMed: Vela-Amieva 2024 Familial case (brother affected: died at 04m) M no Mexico Mexican - - - - MSUD1B Moderate intellectual disability, distal lower limb hypertrophy BCKDHB BCKDHB 2 1 Miriam Erandi Reyna-Fabián
00451632 3bINP-066 PubMed: Vela-Amieva 2024 Familial case (sister affected: died at 07m) M yes Mexico Mexican - - - - MSUD1B Mild intellectual disability, scoliosis, clubfoot BCKDHB BCKDHB 1 1 Miriam Erandi Reyna-Fabián
00451640 3bINP-077 PubMed: Vela-Amieva 2024 - F no Mexico Mexican - - - - MSUD1B Mild intellectual disability BCKDHB BCKDHB 2 1 Miriam Erandi Reyna-Fabián
00451644 3bINP-080 PubMed: Vela-Amieva 2024 Parents with inbreeding and consanguinity (not molecularly tested) F yes Mexico Mexican - - - - MSUD1B Severe intellectual disability, Seizures, Spasticity, Congenital hip dislocation. BCKDHB BCKDHB 1 1 Miriam Erandi Reyna-Fabián
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