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GM22937 LCL from B-Lymphocyte

Description:

CHROMOSOME 1P36 DELETION SYNDROME

Affected:

Yes

Sex:

Female

Age:

No Data

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Chromosome Abnormalities
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Country of Origin USA
Relation to Proband proband
Confirmation Karyotypic analysis after cell line submission to CCR
ISCN 46,XX,del(1)(p36.3),9qh-.arr[hg19]1p36.33p36.22 (721289-10032216) X1
Species Homo sapiens
Common Name Human
Remarks Clinically affected; large anterior fontanelle; ears are low-set with thickened ear helices, posteriorly rotated, and abnormally convoluted; small palpebral fissures; midface hypoplasia; flat nasal bridge; prominent occiput; high forehead; broad base of nose; micrognathia; left single palmar crease; left pes cavus; axial hypotonia; structural congenital heart defects; transitory hypothyrodism; pubertal changes - tanner 2 at six months of age; prominent ventricles; hydrocephalus; bilateral colpocephaly; abnormal myelination of the anterior limb of the internal capsule; skeletal survery showed decreased ossification of the skull and cervical spine; procedures include cleft palate repair; 9.7 MB deletion of chromosome 1p36 (84A14 deleted, de novo, apparently simple terminal truncation).

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Cytogenetics Chromosome 1: DELETION Aneuploid Segment (-) ish del(1)(:p36.33->qter)

Phenotypic Data

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Demographic Data
Relation to Proband proband
Sex Female
Country USA
 
Data Elements
Clinical Element Type: 1p36 Deletion Syndrome
  (Baseline)
Inheritance
De novo  Unknown
If no, give parental origin  Paternal
Maternal age at time of delivery  30
Rearrangement  Terminal
Deletion Size in Mb  10
Dysmorphic Features
Large anterior fontanelle  Yes
Microcephaly  No
Brachycephaly  No
Low hairline  Unknown
Small ears  No
Low-set ears  Yes
Ear asymmetry  No
Thickened ear helices  Yes
Synophrys  No
Deep-set eyes  No
Hypertelorism  No
Small palpebral fissures  Yes
Upslanting palpebral fissures  No
Downslanting palepebral fissures  No
Midface hypoplasia  Yes
Flat nasal bridge  Yes
Pointed chin  No
Clinodactyly  No
Neurological
Mental retardation  No
Developmental delay  Unknown
Speech delay  Unknown
Seizures  No
Epileptic encephalopathy  No
Hypotonia  Yes
Feeding difficulties  No
Oropharyngeal dysphasia  No
Self-abusive behavior  No
Cardiovascular
Cardiomyopathy  No
Structural congenital heart defects  Yes
Patent foramen ovale  No
Patent ductus arteriosus  No
Ventricular septal defects  No
Atrial septal defect  No
Ebstein anomaly  No
Bicommisural aortic valve  No
Ophthalmologic and Audiologic
Hypermetropia (farsightedness)  No
Myopia  No
Strabismus  No
Visual inattentiveness  No
Hearing problems  No
Conductive hearing loss  No
Sensorineural hearing loss  No
Gastrointestinal
Constipation  No
Reflux  No
Ulcer  No
Hiatal hernia  No
Discomfort  No
Endocrine
Thryroid function studies  Yes
Pubertal changes  Yes
MRI Abnormalities
Polymicrogyria  No
Leukoencephalopathy  No
Generalized atrophy  No
Prominent ventricles  Yes
Remarks Clinically affected; large anterior fontanelle; ears are low-set with thickened ear helices, posteriorly rotated, and abnormally convoluted; small palpebral fissures; midface hypoplasia; flat nasal bridge; prominent occiput; high forehead; broad base of nose; micrognathia; left single palmar crease; left pes cavus; axial hypotonia; structural congenital heart defects; transitory hypothyrodism; pubertal changes - tanner 2 at six months of age; prominent ventricles; hydrocephalus; bilateral colpocephaly; abnormal myelination of the anterior limb of the internal capsule; skeletal survery showed decreased ossification of the skull and cervical spine; procedures include cleft palate repair; 9.7 MB deletion of chromosome 1p36 (84A14 deleted, de novo, apparently simple terminal truncation).

Publications

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Gajecka M, Mackay KL, Shaffer LG, Monosomy 1p36 deletion syndrome American journal of medical genetics Part C, Seminars in medical genetics145C:346-56 2007
PubMed ID: 17918734

External Links

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NCBI GTR 607872 CHROMOSOME 1p36 DELETION SYNDROME
OMIM 607872 CHROMOSOME 1p36 DELETION SYNDROME
Omim Description MONOSOMY 1p36 SYNDROME

Images

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View FISH Spectrum Green detects CEB108/T7,Texas Red detects SKI, DAPI counterstain
karyotype Spectrum Green detects CEB108/T7,Texas Red detects SKI, DAPI counterstain

Culture Protocols

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Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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