PIGMENTARY ABNORMALITIES AND CHROMOSOMAL AND GENETIC MOSAICISM AND CHIMERISM

Mosaicism, chimerism and sex-chromosome inactivation.

fluoride and dental fluorosis and treatment

چکیده ندارد.

REVIEW Chromosomal and genetic abnormalities in myeloma

Chromosomal translocations are a hallmark of lymphoid tumours. Multiple myeloma (MM) is a tumour of the plasma cell, the terminally differentiated B lymphoid cell. In recent years, a large number of chromosomal and genetic abnormalities have been detected in myeloma, the most prominent being chromosome 13q deletions and translocations affecting the immunoglobulin heavy chain (IgH) locus on chro...

Association of Fetal and Parental Chromosomal Abnormalities with Congenital Anomalies

Background & Aims: Chromosome abnormalities are a major cause of miscarriage and neonatal mortality. The present study aimed to determine the association of fetal and parents chromosomal abnormalities with congenital anomalies. Methods: A cross-sectional study was performed in a tertiary referral center (Afzalipour Hospital) over 16 months period (2011-2012). The study groups consisted of 77 fe...

Clinical patterns of pigmentary mosaicism - our experience

Pigmentary mosaicisms are nevoid diseases characterized by the presence on the skin of hyperor hypopigmented macules with particular clinical patterns. Occasionally they show association with extracutaneous defects that may alter the normal development of the affected person. We present a compilation of all the cases of pigmentary mosaicism evaluated at our Department in the past decade (Dermat...