GM22910
LCL from B-Lymphocyte
Description:
CHROMOSOME 1P36 DELETION SYNDROME
CHROMOSOME DELETION
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
|
Relation to Proband
|
proband
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
46,XY,del(1)(p36.3).arr 1p36.33p36.31(51585-6551624)x1
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by LINE assay |
|
Cytogenetics |
Chromosome 1: DELETION Aneuploid Segment (-)del(1)(:p36.33>qter) |
Demographic Data |
Relation to Proband |
proband |
Sex |
Male |
|
Data Elements |
Clinical Element Type: 1p36 Deletion Syndrome |
(Baseline) |
Inheritance |
De novo |
Unknown |
If no, give parental origin |
Paternal |
Rearrangement |
Terminal |
Deletion Size in Mb |
6.5 |
Dysmorphic Features |
Large anterior fontanelle |
No |
Microcephaly |
Unknown |
Brachycephaly |
Unknown |
Low hairline |
Unknown |
Small ears |
Yes |
Low-set ears |
Yes |
Ear asymmetry |
Yes |
Thickened ear helices |
Yes |
Synophrys |
No |
Deep-set eyes |
Yes |
Hypertelorism |
Yes |
Small palpebral fissures |
Yes |
Upslanting palpebral fissures |
No |
Downslanting palepebral fissures |
Yes |
Midface hypoplasia |
No |
Flat nasal bridge |
Yes |
Pointed chin |
Yes |
Clinodactyly |
Unknown |
Neurological |
Mental retardation |
Unknown |
Developmental delay |
Unknown |
Speech delay |
Unknown |
Seizures |
Unknown |
Epileptic encephalopathy |
Unknown |
Hypotonia |
Unknown |
Feeding difficulties |
Unknown |
Oropharyngeal dysphasia |
Unknown |
Self-abusive behavior |
No |
Cardiovascular |
Cardiomyopathy |
Unknown |
Structural congenital heart defects |
Unknown |
Patent foramen ovale |
Unknown |
Patent ductus arteriosus |
Unknown |
Ventricular septal defects |
Unknown |
Atrial septal defect |
Unknown |
Ebstein anomaly |
Unknown |
Bicommisural aortic valve |
Unknown |
Ophthalmologic and Audiologic |
Hypermetropia (farsightedness) |
Unknown |
Myopia |
Unknown |
Strabismus |
No |
Visual inattentiveness |
Unknown |
Hearing problems |
Unknown |
Conductive hearing loss |
Unknown |
Sensorineural hearing loss |
Unknown |
Gastrointestinal |
Constipation |
Yes |
Reflux |
No |
Ulcer |
No |
Hiatal hernia |
No |
Discomfort |
No |
Endocrine |
Thryroid function studies |
Unknown |
Pubertal changes |
No |
MRI Abnormalities |
Polymicrogyria |
Unknown |
Leukoencephalopathy |
Unknown |
Generalized atrophy |
Unknown |
Prominent ventricles |
Unknown |
Remarks |
Small ears; low-set ears; ear asymmetry; thickened ear helices; slight deep-set eyes; slight hypertelorism; slight small palpebral fissures; downslanting palepebral fissures; flat nasal bridge; pointed chin; constipation. |
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
PubMed ID: 23665875 |
|
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 |
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 |
- |
|
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