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GM28037 Fibroblast from Skin, Skin

Description:

LEIGH SYNDROME; LS
SURFEIT 1; SURF1

Affected:

Yes

Sex:

Female

Age:

6 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
Biopsy Source Skin
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Skin
Race White
Ethnicity Not Hispanic/Latino
Ethnicity Australian
Country of Origin AUSTRALIA
Family History N
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks See "Phenotypic Data" tab

Characterizations

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PDL at Freeze 4.67
Passage Frozen 2
 
Gene SURF1
Chromosomal Location 9q34.2
Allelic Variant 1 Tyr117*; LEIGH SYNDROME
Identified Mutation C.351T>G (p.Tyr117*)
 
Gene SURF1
Chromosomal Location 9q34.2
Allelic Variant 2 p.Leu105Serfs*14; LEIGH SYNDROME
Identified Mutation c.312_321del10insAT (p.Leu105Serfs*14)

Phenotypic Data

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Demographic Data
Relation to Proband proband
Age at Sampling 6 YR
Sex Female
Age of Onset(If not a control) 18 MO
Age at Diagnosis(If not a control) 2 YR
Hispanic or Latino/Not Hispanic or Latino Not Hispanic/Latino
Racial Category White
Country AUSTRALIA
 
Data Elements
Clinical Element Type: General NIGMS Catalog Remarks
  (Baseline)
Mutation Information
Gene, variant, consequence, and exon number:  PATHOGENIC VARIANTS IN SURF1, NM_003172.3: C.351T>G (P.TYR117*), C.312_321 DEL10INSAT(P.LEU105SERFS*14)
Zygosity:  Heterozygous
Age of Symptom Onset and Age at Diagnosis
Age of Symptom Onset:  18 MONTHS
Age at Diagnosis:  2 YEARS
In Utero History Information
Birth History Information
Additional Information:  MOTHER INDUCED AT 38 WEEKS DUE TO PREGNANCY-INDUCED HYPERTENSION
Dysmorphic Features
Additional Information:  BILATERAL PTOSIS (RESOLVED AT 3 YRS); HYPERTRICHOSIS
Neurological Symptoms
Ataxia
Hypotonia
Unstable gait
White matter issues
Additional Information:  UNSTABLE WALK, BROADBASED GAIT, TREMOR
Optical and Audiological Symptoms
Nystagmus
Additional Information:  VERTICAL NYSTAGMUS
Musculoskeletal Symptoms
Additional Information:  SHORT STATURE
Developmental Milestones
Delayed speech and language development
Abnormal height for age
Abnormal weight for age
Sitting Without Assistance:  Achieved but not maintained
Walking Without Assistance:  Not achieved and not maintained
Additional Information:  SOME CRAWLING; AFTER SEPSIS (STREP A) AT 3 YEARS: LOST ABILITY TO WALK/SIT/STAND UNAIDED, MORE HYPOTONIC, LOST HEAD AND FINE MOTOR CONTROL, HAD TREMORS, DROOLED; NOW: SITS SUPPORTED, DEVELOPMENTAL GAINS, GOOD FINE MOTOR FUNCTION, CLIMBS
Gastrointestinal Symptoms
Gastrointestinal reflux
Additional Information:  REFLUX, MILD-MODERATE OROPHARYNGEAL DYSPHAGIA
Genitourinary Symptoms
Respiratory and Cardiovascular Symptoms
Cognitive and Behavioral Symptoms
Happy personality
Additional Information:  EXTREMELY SOCIABLE
Additional Information
Uncategorized Symptoms:  AT 3 YEARS, WEIGHT: 3RD TO 5TH %ILE, HEIGHT: 2ND %ILE, HEAD CIRCUMFERENCE: 45TH %ILE; FULL EYE MOVEMENTS BUT HAD VERTICAL NYSTAGMUS, VISUALLY AWARE, BROAD-BASED GAIT, NEGATIVE GOWERS SIGN; REASONABLE STRENGTH, DEPRESSED KNEE AND ANKLE RELEXES, SHORT STATURE
Testing Performed
Neurological Testing:  MRI
Optical and Audiological Testing:  GOOD HEARING; HORIZONTAL NYSTAGMUS, RIGHT AND LEFT GAZE, AND VERTICAL NYSTAGMUS AT 5 YEARS
Treatments and Assistive Devices
Occupational therapy
Physical therapy
Speech therapy
Wheelchair or ambulation devices
Additional Testing:  GAIT TRAINER; STANDING FRAME; IMPROVED SPEECH AND FINE MOTOR SKILLS WITH THERAPY
Medications
 RIBOFLAVIN, THIAMINE, CO-ENZYZME, OMEPRAZOLE, OCCASIONAL GAVISCON, VITAMIN E, ALPHA-LIPOIC ACID, BIOTIN, FOLINIC ACID, VITAMIN C, VITAMIN D, PROBIOTIC, MULTIVITAMIN, PEDIASURE
Family History
Remarks See "Phenotypic Data" tab

External Links

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Gene Cards MTATP6
SURF1
Gene Ontology GO:0004129 cytochrome-c oxidase activity
GO:0005739 mitochondrion
GO:0005746 mitochondrial electron transport chain
GO:0006118 electron transport
GO:0008535 cytochrome c oxidase biogenesis
GO:0009060 aerobic respiration
GO:0016021 integral to membrane
GO:0019866 inner membrane
NCBI Gene Gene ID:6834
NCBI GTR 185620 SURFEIT 1; SURF1
256000 LEIGH SYNDROME; LS
OMIM 185620 SURFEIT 1; SURF1
256000 LEIGH SYNDROME; LS
Omim Description LEIGH SYNDROME
  NECROTIZING ENCEPHALOPATHY, INFANTILE SUBACUTE, OF LEIGH; SNE

Culture Protocols

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Cumulative PDL at Freeze 4.67
Passage Frozen 2
Split Ratio 1:2
Temperature 37 C
Percent CO2 5%
Percent O2 3%
Medium Eagles Minimum Essential Medium with Earle's salts:Dulbecco's modified MEM 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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