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Quran and 
Determination of Sex 
by Dr. Ibrahim B. Syed 
  The Noble Qur'an 
which was revealed to Prophet Muhammad(pbuh) about 1400 years ago mentions how 
the sex of a human being is determined. The following two verses or Ayat of the 
Qur'an are very clear on this matter.(A. Yusuf Ali translation) 
                                                "And of him He made  
                                                Two sexes, male and female."   
Surah Qiyamat (the Resurrection), 75: 39   In the above 
Ayah, " of him He made two sexes, male and female" means that of  the human male 
(he), He (Allah) Created both the 
sexes male and female.  Hence   human male is responsible for the birth of a 
male child or a female child.  The human female is not responsible for the sex 
determination of the child.  However, in many Muslim countries the woman is 
blamed for the birth of a female child as in these countries they welcome the 
arrival of a male child. 
                                                "That He did create in 
pairs,-male and female, 
                                                   From a seed when lodged (in 
its place);  Surah Najm(the Star) 53:45-46   To understand 
Sex determination we need to understand the Chromosomes, particularly the X and 
Y chromosomes. The accepted 
chromosome number for humans in 1935 was forty-eight. The year 1956 is 
considered to mark the beginning of modern human Cytogenetics. Until this time 
the number of chromosomes in the normal human cell was considered to be 48. 
Due to improvements in techniques it was discovered that the correct number is 
46 (Tjio and Levan, 1956)  Reference: 
Tjio JH, Levan A (1956) The chromosome number of man. Am J Obstet Gynecol 
130:723-724    What is a 
Chromosome?  A chromosome is 
composed of a very long molecule of DNA and associated proteins that carry 
hereditary information. The centromere, which is at the center of the 
chromosome, is a specialized structure that appears during cell division and 
ensures the correct distribution of duplicated chromosomes to daughter cells. 
Telomeres are the structures that seal the end of a chromosome. Telomeres play a 
critical role in chromosome replication and maintenance by counteracting the 
tendency of the chromosome to otherwise shorten with each round of replication. Chromosomes are 
composed of protein and DNA, and they are distinct dense bodies found in the 
nucleus of cells. Genetic information is contained in the DNA of chromosomes in 
the form of linear sequences of bases (A, T, C, G). The DNA in an individual 
chromosome is one, long molecule, which is highly coiled and condensed. The 
total number of bases in all the chromosomes of a human cell is approximately 
six billion and individual chromosomes range from 50 to 250 million bases. The 
DNA sequence for a single trait is called a gene. Each chromosome contains a few 
thousand genes, which range in size from a few thousand bases up to 2 million 
bases.   During most of 
the cell cycle, interphase, the chromosomes are somewhat less condensed and are 
not visible as individual objects under the light microscope. However during 
cell division or mitosis, the chromosomes become highly condensed and are then 
visible as dark distinct bodies within the nuclei of cells. The chromosomes are 
most easily seen and identified at the metaphase stage of cell division.   Sex 
Chromosomes X and Y 
 Somatic cell  
is any cell other than a sperm or egg cell. Somatic cells in humans and most 
other animals are diploid. Diploid cells  are cells containing two 
sets of chromosomes.    Each somatic cell in humans contains 46  
chromosomes which can be distinguished from one another by their appearance 
under a microscope. Chromosomes differ in size, position of the centromere, and 
staining pattern.  A pair of chromosomes that have the same size, centromere 
position and staining pattern are called Homologous chromosomes (homologues). 
The chromosomes of a homologous pair carry genes controlling the same inherited 
traits. Each locus (the position of a gene along the length of a chromosome) is 
in the same position on homologues.  One exception to 
homologous chromosomes for human somatic cells is the two distinct sex 
chromosomes which are important in sex determination. All other chromosomes 
are referred to as autosomes. Sex 
chromosomes in humans are the X and Y chromosomes. 
 
 
 
 The special type 
of cell division that produces haploid cells is called meiosis and 
occurs only in the gonads (ovaries of the female and testes of the male). 
Meiosis in humans produces sperm and egg cells which contain 23 chromosomes. 
When fertilization occurs, the zygote contains 46 chromosomes and is diploid. 
The process of meiosis and fertilization are unique to sexual reproduction and 
all sexually reproducing organisms follow a basic pattern of alternation between 
diploid and haploid conditions. Haploid cell  is a cell that contains a 
single chromosome set. The number of 
chromosomes in human cells is 46 with 22 autosomal pairs (a total of 44) (one of 
each type contributed by the mother and one of each type from the father) and 2 
sex chromosomes - 2 X chromosomes for females (one from father and one from 
mother) or an X and a Y chromosome for males (the X from the mother and the Y 
from the father). Sex 
chromosomes determine the sex of an organism and some other sex-linked 
characteristics. In the process 
of reproduction, special cells are produced in males and females. Males 
produce sperm cells and females produce egg cells, or ova. The chromosomal 
makeup of these cells is interesting. Each sex cell from each parent contains 
only one member from each pair of chromosomes. Therefore, in ova or egg cells 
there are 22 autosomes plus an X chromosome. There are two types of sperm cells, 
each type carrying 22 autosomes plus a gender-determining chromosome, i.e., X or 
Y. The banding of 
chromosomes by using dyes was discovered in the late 1960's and before that 
cytogeneticists depended on chromosome length and position of a constriction to 
identify the individual chromosomes. The band width and the order of bands is 
characteristic of a particular chromosome - a trained cytogeneticist can 
identify each chromosome (1,2,3...22, X and Y) by observing its banding pattern 
under the microscope. 
 Sperm and egg 
cells are called gametes and are distinct from somatic cells with 
respect to their chromosome number.  Each human gamete contains a single set of 
22 autosomes and a sex chromosome (either an X or a Y). Gametes in humans and 
other organisms are haploid.   Haploid 
number: The number of 
chromosomes in a haploid cell (designated N). The haploid number of humans is 
23. Sexual intercourse allows a haploid sperm cell from the father to reach and 
fuse with an egg cell from the mother in a process called fertilization.
Fertilization is the fusion of a sperm cell and an egg cell to form a 
zygote.  Zygote  
is a fertilized egg cell  and it contains the two haploid sets of chromosomes 
from the gametes and is diploid. 
 Half of the 
genes carried on the chromosomes are contributed by the mother (set of 
chromosomes from the egg cell) and half by the father (set of chromosomes from 
the sperm cell). During 
development from a zygote to a sexually mature adult, the zygote's genetic 
information is passed with precision to all somatic cells by the process of 
mitosis. Sex organs, which form during development, then produce new gametes 
which can initiate a new cycle. A human's sex is 
predetermined in the sperm gamete (spermatozoa).  The egg gamete mother cell is 
said to be homogametic, because all its cell possess the XX sex chromosomes. 
Sperm gametes are deemed heterogametic because around half of them contain the X 
chromosome and others possess the Y chromosome to compliment the first X 
chromosome. In light of this, there are two possibilities that can occur during 
fertilization between male and female gametes, XX and XY. Since sperm are the 
variable factor (i.e. which sperm fertilizes the egg) they are responsible for 
determining sex. Chromosomes X 
and Y Chromosomes X 
and Y do not truly make up a homologous pair. They act similarly in their roles, 
but they are not homologous (the same). The X chromosome in humans is much 
longer than the Y chromosome and also contains many more genes. These genes are 
said to be sex linked, due to the fact they are present in one of the sex 
chromosomes. During fertilization, when the opposing homologous chromosomes come 
together, the smaller Y chromosome offers no dominance against the 'extra' 
X-chromosomes as indicated below. Sex Linked 
Characteristics These sex linked 
genes on the X chromosome display a number of characteristics. The following are 
some examples of phenotypes as a result of these genes: Red-Green colour 
blindness and  Hemophilia - (a condition which prevents the clotting of the 
blood)   Humans usually 
have 46 chromosomes per diploid cell consisting of 22 sets of autosomes 
and a set of sex chromosomes - either XX or XY. In the 
usual course of events, individuals with the karyotype 46, XX are 
female and individuals with 46, XY, are male. 
   Chromosome 
Constitution       Name of Syndrome                 Sex of Individual      
Frequency in Population             46, 
XX                            Normal                                       
Female                                 0.511 *             46, 
XY                        Normal                                       
Male                                    0.489*             45, 
XO                            Turner's Syndrome                     
Female                                1 in 5,000             47, 
XXY                          Klinefelter's Syndrome              
Male                                   1 in 700 
____________________________________________________________________________________________ * Female (46, 
XX) and Male (46, XY) frequencies taken from US Census projection of July 1, 
1966 with no correction for chromosome constitution. It is clear that 
the presence of a Y chromosome is necessary for male sexual 
characteristics to develop. 
                 
EGG                             
SPERM                                                
    EGG                                   SPERM 
 
                                       
 
 
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