Dr. Ignatia B Van den veyver MD
OB-GYN (Obstetrician-Gynecologist) | Maternal & Fetal Medicine
6620 Main St Suite 1450 Houston TX, 77030About
Dr. Ignatia Van den veyver is an obstetrician-gynecologist practicing in Houston, TX. Dr. Van den veyver specializes in women's health, particularly the female reproductive system, pregnancy and childbirth. As an obstetrician-gynecologist, or OB-GYN, Dr. Van den veyver can treat a number of health issues related to the vagina, uterus, ovaries, fallopian tubes and breasts. Dr Van den veyver can also treat women during pregnancy, labor, childbirth and the postpartum period. In this specialty, doctors focus on reproductive care from puberty through adulthood.
Education and Training
Univ Instelling Antwerpen- Fac Voor Geneeskunde En Farm- Wilrijk 1986
Universitair Instelling Antwerpen 1986
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3.
- Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
- Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter.
- Methyl-CpG-binding protein 2 mutations in Rett syndrome.
- Terminal osseous dysplasia and pigmentary defects: clinical characterization of a novel male lethal X-linked syndrome.
- Skewed X inactivation in X-linked disorders.
- Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice.
- The human homologue (PEG3) of the mouse paternally expressed gene 3 (Peg3) is maternally imprinted but not mutated in women with familial recurrent hydatidiform molar pregnancies.
- Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.
- Genetic effects of methylation diets.
- Genetic basis of Rett syndrome.
- Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome.
- Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?
- The product of the imprinted gene IPL marks human villous cytotrophoblast and is lost in complete hydatidiform mole.
- Recurrent pregnancy loss due to familial and non-familial habitual molar pregnancy.
Dr. Ignatia B Van den veyver MD's Practice location
Practice At 6620 Main St Suite 1450
6620 Main St Suite 1450 -Houston, TX 77030Get Direction
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