Daily tips on pregnacy and conception

Daily tips on pregnacy and conception -Pregnancy counseling
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Cerebral palsy (CP) is a group of disorders affecting movement and posture, stemming from brain damage occurring before,...
12/07/2025

Cerebral palsy (CP) is a group of disorders affecting movement and posture, stemming from brain damage occurring before, during, or shortly after birth. In babies, CP may manifest as developmental delays, unusual muscle tone (either too stiff or too floppy), and difficulties with movement and posture. While the brain damage doesn't progress, the symptoms can change over time as the child grows and develops.

Encephalocele is a neural tube defect characterized by sac-like protrusions of the brain and the membranes that cover it...
12/07/2025

Encephalocele is a neural tube defect characterized by sac-like protrusions of the brain and the membranes that cover it through openings in the skull. These defects are caused by failure of the neural tube to close completely during fetal development. Encephaloceles cause a groove down the middle of the skull, or between the forehead and nose, or on the back side of the skull. The severity of encephalocele varies, depending on its location.[1]

The success rate of IUCD(Intrauterine contraceptive device) also referred to as IUD(Intrauterine device) is 99.2-99.8% t...
18/05/2025

The success rate of IUCD(Intrauterine contraceptive device) also referred to as IUD(Intrauterine device) is 99.2-99.8% the other 0.2- O.8% is for cases as seen below

Baby delivered with an IUD on the back

Hemolytic disease of the newborn (HDN) is a blood disorder in a fetus or newborn infant. In some infants, it can be fata...
11/08/2024

Hemolytic disease of the newborn (HDN) is a blood disorder in a fetus or newborn infant. In some infants, it can be fatal.

Normally, red blood cells (RBCs) last for about 120 days in the body. In this disorder, RBCs in the blood are destroyed quickly and thus do not last as long.

Causes
During pregnancy, RBCs from the unborn baby can cross into the mother's blood through the placenta. HDN occurs when the immune system of the mother sees a baby's RBCs as foreign. Antibodies then develop against the baby's RBCs. These antibodies attack the RBCs in the baby's blood and cause them to break down too early.

HDN may develop when a mother and her unborn baby have different blood types. The types are based on small substances (antigens) on the surface of the blood cells.

There is more than one way in which the unborn baby's blood type may not match the mother's.

A, B, AB, and O are the 4 major blood group antigens or types. This is the most common form of a mismatch. In most cases, this is not very severe.
Rh is short for the "rhesus" antigen or blood type. People are either positive or negative for this antigen. If the mother is Rh-negative and the baby in the womb has Rh-positive cells, her antibodies to the Rh antigen can cross the placenta and cause very severe anemia in the baby. It can be prevented in most cases.
There are other, much less common, types of mismatch between minor blood group antigens. Some of these can also cause severe problems.

Preeclampsia :A potentially dangerous pregnancy complication characterised by high blood pressure.Pre-eclampsia usually ...
02/07/2022

Preeclampsia :

A potentially dangerous pregnancy complication characterised by high blood pressure.
Pre-eclampsia usually begins after 20 weeks of pregnancy in a woman whose blood pressure had been normal. It can lead to serious, even fatal, complications for both mother and baby.

Symptoms:
Requires a medical diagnosis
There may be no symptoms. Others include ,High blood pressure and protein in the urine are key features. There may also be swelling in the legs and water retention, but this can be hard to distinguish from normal pregnancy.

Down Syndrome A genetic chromosome 21 disorder causing developmental and intellectual delays.Down's syndrome is a geneti...
01/06/2022

Down Syndrome

A genetic chromosome 21 disorder causing developmental and intellectual delays.
Down's syndrome is a genetic disorder caused when abnormal cell division results in extra genetic material from chromosome 21.

Spinal BifidaA birth defect in which a developing baby's spinal cord fails to develop properly.It occurs when a developi...
25/05/2022

Spinal Bifida
A birth defect in which a developing baby's spinal cord fails to develop properly.
It occurs when a developing baby's spinal cord fails to develop or close properly while in the womb.
Causes:
It's thought to result from a combination of genetic, nutritional and environmental risk factors, such as a family history of neural tube defects and folate (vitamin B-9) deficiency

Uterus didelphys (sometimes also uterus didelphis) represents a uterine malformation where the uterus is present as a pa...
23/03/2022

Uterus didelphys (sometimes also uterus didelphis) represents a uterine malformation where the uterus is present as a paired organ when the embryogenetic fusion of the Müllerian ducts fails to occur. As a result, there is a double uterus with two separate cervices, and possibly a double va**na as well. Each uterus has a single horn linked to the ipsilateral fallopian tube that faces it

The term "fetal macrosomia" is used to describe a newborn who's much larger than average.A baby who is diagnosed as havi...
26/02/2022

The term "fetal macrosomia" is used to describe a newborn who's much larger than average.

A baby who is diagnosed as having fetal macrosomia weighs more than 8 pounds, 13 ounces (4,000 grams), regardless of his or her gestational age.
Signs include;
Large fundal height.

Excessive amniotic fluid (polyhydramnios). Having too much amniotic fluid
Risk Factors:
Obesity,gestational diabetes,excessive weight gain during pregnancy, and overdue pregnancy.
Complications...
Labour problems ,ge***al track lacerations ,uterine rupture ,bleeding after delivery.The new born is at risky of have hyperglycemia and consequently shock and death ..

Drinking water doing pregnancy is very important it prevent complications  like Oligohydramnios, dehydration,Intrauterin...
22/10/2021

Drinking water doing pregnancy is very important it prevent complications like Oligohydramnios, dehydration,
Intrauterine Growth Restriction (IUGR),
Preterm birth,
Labor complications such as cord compression, meconium-stained fluid, and cesarean delivery.

What is oligohydramnios??Oligohydramnios is the condition of having too little amniotic fluid.  Medical professionals ca...
22/10/2021

What is oligohydramnios??
Oligohydramnios is the condition of having too little amniotic fluid. Medical professionals can measure the amount of fluid through a few different methods, most commonly through amniotic fluid index (AFI) evaluation or deep pocket measurements. If an AFI shows a fluid level of fewer than 5 centimeters (or less than the 5th percentile), the absence of a fluid pocket 2-3 cm in-depth, or a fluid volume of less than 500mL at 32-36 weeks gestation, then a diagnosis of oligohydramnios would be suspected.

Complications include;;
Birth defects – Problems with the development of the kidneys or urinary tract which could cause little urine production, leading to low levels of amniotic fluid.
Placental problems – If the placenta is not providing enough blood and nutrients to the baby, then the baby may stop recycling fluid.
Leaking or rupture of membranes –This may be a gush of fluid or a slow constant trickle of fluid. This is due to a tear in the membrane. Premature rupture of membranes (PROM) can also result in low amniotic fluid levels.
Post Date Pregnancy– A postdate pregnancy (one that goes over 42 weeks) can have low levels of amniotic fluid, which could be a result of declining placental function.
Maternal Complications– Factors such as maternal dehydration, hypertension, preeclampsia, diabetes, and chronic hypoxia can have an effect on amniotic fluid levels.

PROGERIA;Progeria ,also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that ca...
31/08/2021

PROGERIA;
Progeria ,also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life.

Children with progeria generally appear normal at birth. During the first year, signs and symptoms, such as slow growth and hair loss, begin to appear. Heart problems or strokes are the eventual cause of death in most children with progeria. The average life expectancy for a child with progeria is about 13 years. Some with the disease may die younger and others may live longer, even up to 20 years.

There's no cure for progeria, but ongoing research shows some promise for treatment.

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