SNPMiner Trials by Shray Alag


SNPMiner Trials: Mutation Report


Report for Mutation P250R

Developed by Shray Alag, 2019.
SNP Clinical Trial Gene

There is one clinical trial.

Clinical Trials


1 Clinical Study of Muenke Syndrome (FGFR3-Related Craniosynostosis)

This study will explore the range and type of medical and developmental problems in patients with Muenke syndrome, a condition that results when one or more of the suture between the bones of the skull close before birth. Because of the premature closure, the skull is not able to grow in its natural shape; instead, it compensates with growth in areas of the skull where the sutures have not yet closed. This can result in an abnormally shaped head, wide-set eyes, and flattened cheekbones. Patients may also have an enlarged head, abnormalities of the hands or feet, and hearing loss. The fibroblast growth factor receptor 3 (FGFR3) gene, which is involved in the development and maintenance of bone tissue, plays a role in Muenke syndrome. In some cases, the FGFR3 mutation is inherited from a parent with Muenke syndrome; in other cases, where there is no family history of the disorder, the mutation occurs anew. A better understanding of this gene may lead researchers to develop better treatments and genetic counseling for people affected by Muenke syndrome. Patients with Muenke syndrome and their blood relatives may be eligible for this study. Family members with confirmed Muenke syndrome will have genetic counseling, and patients undergo the following tests and procedures: - Review of medical records and test results. - Questionnaires about the patient's prenatal, birth, newborn, and past medical history; family history; growth and development; medications; and current therapies. - Physical, neurological, ear, nose and throat, dental, and eye examinations. - Neuropsychological testing to assess cognitive thinking abilities. - Hearing evaluation. This includes an audiology test in which the patients listens to soft tones through earphones; a power reflectance test in which a chirping sound is heard through an earpiece placed at the entrance to the ear canal, and possibly an ABR/ASSR test, in which electrodes are attached to the forehead, earlobes, and behind the ears to measure brain waves in response to certain conditions. - MRI scan of the brain. MRI uses a strong magnetic field and radio waves to produce detailed pictures of the brain. During the scan, the patient lies on a table in a narrow cylinder (the scanner), wearing ear plugs to muffle loud noises that occur with electrical switching of the magnetic fields. - MRI scan of the middle and inner ear. This test is similar to the MRI, but uses a dye injected in a vein to enhance the images. - CT scan of the skull. CT uses x-rays to produce 3-dimensional images of the part of the body studied. - Dental evaluation with x-rays. - Skeletal survey (x-rays of all bones of the body). - Developmental assessment of IQ testing. - Blood tests for research purposes. A cell line may be established for use in future research. - Medical photographs to demonstrate clinical features, including side and front views of the face, head, and other parts of the body that may be involved in Muenke syndrome, like the hands and feet. - Other consultations or tests as clinically indicated

NCT00106977 Craniosynostosis Muenke Syndrome
MeSH: Syndrome Craniosynostoses
HPO: Brachycephaly Craniosynostosis Lambdoidal craniosynostosis Metopic synostosis Oxycephaly Premature closure of fontanelles Scaphocephaly Trigonocephaly Turricephaly

The objective of this study is primarily to increase our understanding of the genetics and clinical characteristics of Muenke syndrome.. - INCLUSION CRITERIA: Subjects who have had confirmation of a Pro250Arg mutation in FGFR3 by a CLIA-certified laboratory. --- Pro250Arg ---

Geneticists and genetic counselors may refer individuals who are suspected to have Muenke syndrome, but who have not yet been tested for the FGFR3 Pro250Arg mutation. --- Pro250Arg ---

Testing for the Pro250Arg mutation maybe performed at the discretion of our research group. --- Pro250Arg ---

- INCLUSION CRITERIA: Subjects who have had confirmation of a Pro250Arg mutation in FGFR3 by a CLIA-certified laboratory. --- Pro250Arg ---

Primary Outcomes

Description: The objective of this study is primarily to increase our understanding of the genetics and clinical characteristics of Muenke syndrome.

Measure: Understanding

Time: Ongoing


HPO Nodes


Craniosynostosis
Genes 124
RAB23 TLK2 KRAS SLC25A24 SLC12A6 IL11RA DPH1 FLNA FLNB MYH3 IFT140 MASP1 FAT4 COL10A1 ERCC2 ERCC3 B3GLCT IRX5 TCF12 CENPJ CYP26B1 DONSON ERF COMT ATR ADAMTS3 CENPE LEMD3 SCARF2 ORC6 CWC27 RBBP8 ENPP1 TRAIP GNPTAB APC2 RNF113A KAT6A GLIS3 NSD1 POR TCIRG1 COLEC10 SPECC1L DPF2 RREB1 PTEN SKI GPC6 CCNQ NSUN2 GMNN JMJD1C ALX4 IFT43 RSPRY1 SLC39A8 HNRNPK STAT3 TBC1D24 ZIC1 HIRA TWIST1 PPP1CB CDC45 WDR19 ESCO2 PHEX ORC1 TGFBR1 SLC2A10 MSX2 ORC4 TGFBR2 BMP4 COLEC11 LIG4 SEC24D SETD2 IMPAD1 GTF2E2 TNFSF11 FBN1 IFT52 PPP3CA EFNB1 CEP120 ATRIP SEC24C CLCN7 MEGF8 ARVCF P4HB CCBE1 NFIX GLI3 RECQL4 UFD1 SNX10 WDR35 MPLKIP GTF2H5 LRP5 AKT1 SMO CEP152 FGFR1 IFT122 FGFR3 CDT1 FGFR2 CDC6 DMP1 TMCO1 MAP3K7 PLK4 MED12 CDH11 TBX1 SMAD3 ALPL SON GP1BB PCNT