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GM21894 Fibroblast from Skin, Unspecified

Description:

CAMPOMELIC DYSPLASIA

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 Heritable Diseases
Biopsy Source Unspecified
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Unspecified
Relation to Proband proband
Confirmation Clinical summary/Case history
ISCN 46,XY
Species Homo sapiens
Common Name Human
Remarks Clinically affected; XY female; stillborn with marked polyhydramnios; large head with prominent occiput; examination of the brain showed large lateral ventricles and dilated aqueduct and missing olfactory nerves; wide forehead; small mandible; wideset eyes; flat nasal bridge; short down-slanted palpebral fissures; long philtrum; small mouth with cleft soft palate; lowset ears; short webbed neck; short sternum; tracheal rings were thin and C-shaped; hemorrhagic lungs; scapulae were narrow; short thumbs; femurs were slightly bowed; tibiae markedly bowed; bilateral clubbed feet; enlarged clitoris; ovaries showed some primitive tubular cords resembling immature but dysgenetic testicular tissue; rete testis tubes were present; parents may be consanguineous; two of the father's sisters had one infant each that died in the neonatal period, neither with short limbs

Characterizations

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PDL at Freeze 7.44
Passage Frozen 8
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin confirmed by LINE assay
 

Phenotypic Data

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Remarks Clinically affected; XY female; stillborn with marked polyhydramnios; large head with prominent occiput; examination of the brain showed large lateral ventricles and dilated aqueduct and missing olfactory nerves; wide forehead; small mandible; wideset eyes; flat nasal bridge; short down-slanted palpebral fissures; long philtrum; small mouth with cleft soft palate; lowset ears; short webbed neck; short sternum; tracheal rings were thin and C-shaped; hemorrhagic lungs; scapulae were narrow; short thumbs; femurs were slightly bowed; tibiae markedly bowed; bilateral clubbed feet; enlarged clitoris; ovaries showed some primitive tubular cords resembling immature but dysgenetic testicular tissue; rete testis tubes were present; parents may be consanguineous; two of the father's sisters had one infant each that died in the neonatal period, neither with short limbs

Publications

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Parivesh A, Délot E, Reyes A, Ryan J, Bhattacharya S, Harley V, Vilain E, Reprograming skin fibroblasts into Sertoli cells: a patient-specific tool to understand effects of genetic variants on gonadal development Biology of sex differences15:24 2023
PubMed ID: 38520033
 
Puck SM, Haseltine FP, Francke U, Absence of H-Y antigen in an XY female with campomelic dysplasia Human genetics57:23-7 1981
PubMed ID: 7196381

External Links

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NCBI GTR 114290 CAMPOMELIC DYSPLASIA
OMIM 114290 CAMPOMELIC DYSPLASIA
Omim Description CAMPOMELIC DYSPLASIA
  CMD1; CMPD1SRY-BOX 9, INCLUDED; SOX9, INCLUDED
  SEX REVERSAL, AUTOSOMAL, 1, INCLUDED; SRA1, INCLUDED
  SRY-RELATED HMG-BOX GENE 9, INCLUDED

Images

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View karyotype 
karyotype 

Culture Protocols

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Passage Frozen 8
Split Ratio 1:3
Temperature 37 C
Percent CO2 10%
Percent O2 AMBIENT
Medium Dulbecco Modified Eagles Medium (high glucose) with 2mM L-glutamine or equivalent
Serum 10% fetal bovine serum Not inactivated
Substrate None specified
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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