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GM29359 Fibroblast

Description:

MANNOSIDOSIS, BETA A, LYSOSOMAL; MANSB
MANNOSIDASE, BETA A, LYSOSOMAL; MANBA

Affected:

Yes

Sex:

Female

Age:

14 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
PIGI Consented Sample
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Race White
Ethnicity Not Hispanic/Latino
Country of Origin USA
Family Member 1
Family History N
Relation to Proband proband
Species Homo sapiens
Common Name Human
Remarks See "Phenotypic Data Tab"

Characterizations

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PDL at Freeze 6.38
Passage Frozen 2
 
Gene MANBA
Chromosomal Location 4q24
Allelic Variant 1 ; MANNOSIDASE, BETA A, LYSOSOMAL; MANBA
Identified Mutation c.1540-1541del (p.Val514Cysfs*10)
 
Gene MANBA
Chromosomal Location 4q24
Allelic Variant 1 ; MANNOSIDASE, BETA A, LYSOSOMAL; MANBA
Identified Mutation C.2352_2356del (p.Thr785Leufs*27)

Phenotypic Data

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Demographic Data
Relation to Proband proband
Age at Sampling 14 YR
Sex Female
Hispanic or Latino/Not Hispanic or Latino Not Hispanic/Latino
Racial Category White
Country USA
 
Data Elements
Clinical Element Type: General NIGMS Catalog Remarks
  (Baseline)
Mutation Information
Gene, variant, consequence, and exon number:  MANBA: C.1540-1541DEL (P.VAL514CYSFS*10) MANBA: C.2352_2356DEL (P.THR785LEUFS*27)
Zygosity:  Heterozygous
Age of Symptom Onset and Age at Diagnosis
In Utero History Information
Birth History Information
Dysmorphic Features
Strabismus
Coarse facies
Additional Information:  DENTITION MISALIGNED BUT NORMATIVE; MILD FACIAL DYSMORPHISM; TORTUOUS CONJUNCTIVAL VESSELS; VACUOLATION; WIDE NASAL BRIDGE; RETROGNATHIA
Neurological Symptoms
Hypotonia
Seizures
Sleep abnormalities
Additional Information:  SEIZURES CONTROLLED BY OXCARBAZEPINE - NO EPISODES FOR 7 YRS; MENTAL RETARDATION; GILLES DE LA TOURETTE SYNDROME; PROGRESSIVE DEMYELINATING PERIPHERAL NEUROPATHY BUT RARE; POSSIBLE SLEEP APNEA
Optical and Audiological Symptoms
Defective hearing
Additional Information:  INTERMITTENT ALTERNATING EXOTROPIA; BILATERAL MODERATE TO SEVERE HEARING LOSS
Musculoskeletal Symptoms
Additional Information:  THENAR ATROPHY BUT RARE; HYPOTONIA
Developmental Milestones
Delayed speech and language development
Delayed fine motor skills
Additional Information:  SAYS SINGLE WORDS AND DOES NOT CONJUGATE; IEP IN PLACE AT SCHOOL
Gastrointestinal Symptoms
Constipation
Additional Information:  CONSTIPATION CONTROLLED WITH MIRALAX
Genitourinary Symptoms
Respiratory and Cardiovascular Symptoms
Additional Information:  LACK OF SWEAT AND COLD DIGITALS; ABNORMAL BLOOD PRESSURE
Cognitive and Behavioral Symptoms
Behavioral problems
Autism spectrum disorder
Aggression
Learning disability
Attention deficit hyperactivity disorder
Intellectual Disability:  Moderate
Additional Information:  BEHAVIOR IMPROVED WITH TRILEPTAL; AGGRESSION DUE TO INABILITY TO COMMUNICATE; ADHD CONTROLLED WITH METHYLPHENIDATE; ASD DIAGNOSED 3/28/22
Additional Information
Uncategorized Symptoms:  BRUISES AND SCARS EASILY; ANGIOKERATOMA ON ABDOMEN; ALLERGIC REACTIONS(ITCHING, RASH, AND PRURITIS) TO AUGMENTIN, NEOMYCIN, LATEX, AND NATURAL RUBBER
Testing Performed
Neurological Testing:  MRI: LEUKODYSTROPHY INCLUDING MARKED CEREBRAL WHITE MATTER VOLUME LOSS; MILD SUPRATENTORIAL VENTRICULOMETRY AND DIFFUSE WHITE MATTER SIGNAL ABNORMALITY.
Treatments and Assistive Devices
Hearing aid
Surgeries  ADENOIDECTOMY
Medications
 KLONOPIN 0.5MG; PROBIOTIC; LEXAPRO 10MG; RITALIN 10MG; LOESTIN 24 FE; TRILEPTAL
Family History
Remarks See "Phenotypic Data Tab"

External Links

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Gene Cards MANBA
Gene Ontology GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0004567 beta-mannosidase activity
GO:0005764 lysosome
GO:0005975 carbohydrate metabolism
GO:0006464 protein modification
NCBI Gene Gene ID:4126
NCBI GTR 248510 MANNOSIDOSIS, BETA A, LYSOSOMAL; MANSB
609489 MANNOSIDASE, BETA A, LYSOSOMAL; MANBA
OMIM 248510 MANNOSIDOSIS, BETA A, LYSOSOMAL; MANSB
609489 MANNOSIDASE, BETA A, LYSOSOMAL; MANBA
Omim Description BETA-MANNOSIDASE DEFICIENCYMANNOSIDASE, BETA A, LYSOSOMAL, INCLUDED; MANBA, INCLUDED
  MANNOSIDASE, BETA B, SOLUBLE, INCLUDED; MANBB, INCLUDED
  MANNOSIDOSIS, BETA; MANB1

Culture Protocols

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Cumulative PDL at Freeze 6.38
Passage Frozen 2
Split Ratio 1:6
Temperature 37 C
Percent CO2 5%
Percent O2 3%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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