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	<title>Baby Care &#187; health</title>
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	<link>http://www.ababycare.com</link>
	<description>Complete baby and child care blog</description>
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		<title>IMPERFORATE ANUS</title>
		<link>http://www.ababycare.com/imperforate-anus/</link>
		<comments>http://www.ababycare.com/imperforate-anus/#comments</comments>
		<pubDate>Sat, 18 Jul 2009 09:41:05 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[Imperforate anus]]></category>
		<category><![CDATA[newborn baby]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=175</guid>
		<description><![CDATA[
In rare cases, a baby’s anus is sealed at birth, either because there is a thin membrane of skin over the opening or because the anal canal, which links the rectum with the anus, has not developed. The rectal pouch may be connected to the vagina, urethra, pr bladder, and surgery must be performed at [...]]]></description>
			<content:encoded><![CDATA[<p><img class="size-full wp-image-176 alignnone" style="margin: 10px;" title="Imperforate anus" src="http://www.ababycare.com/wp-content/uploads/2009/07/Imperforate-anus.jpg" alt="Imperforate anus" width="189" height="261" /></p>
<p>In rare cases, a baby’s anus is sealed at birth, either because there is a thin membrane of skin over the opening or because the anal canal, which links the rectum with the anus, has not developed. The rectal pouch may be connected to the vagina, urethra, pr bladder, and surgery must be performed at once. This condition is routinely checked for at every birth, and is treated immediately if present.</p>
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		<title>PYLORIC STENOSIS</title>
		<link>http://www.ababycare.com/pyloric-stenosis/</link>
		<comments>http://www.ababycare.com/pyloric-stenosis/#comments</comments>
		<pubDate>Sat, 18 Jul 2009 09:30:26 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>
		<category><![CDATA[Pyloric stenosis]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=171</guid>
		<description><![CDATA[
In this condition, the pylorus, the passage that leads from the stomach into the small intestine, is narrow because of a thickening of the muscle. The cause is unknown, and it is more common in boys than in girls.

Symptoms usually first appear at two to four weeks, though they can appear earlier or later. The [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignnone size-full wp-image-172" title="Pyloric stenosis" src="http://www.ababycare.com/wp-content/uploads/2009/07/Pyloric-stenosis.jpg" alt="Pyloric stenosis" width="331" height="220" /></p>
<p>In this condition, the pylorus, the passage that leads from the stomach into the small intestine, is narrow because of a thickening of the muscle. The cause is unknown, and it is more common in boys than in girls.</p>
<p><span id="more-171"></span></p>
<p>Symptoms usually first appear at two to four weeks, though they can appear earlier or later. The stomach contracts powerfully in an attempt to force a buildup of food through the narrow pylorus. This is impossible, however, and the contents of the stomach are vomited up so violently that they may be propelled up to 3 feet (1 meter) – projectile vomiting. The baby may also suffer constipation and dehydration. Ultrasound and a barium swallow may be used to confirm the diagnosis. A simple operation to widen the pylorus can be performed, curing the condition completely.</p>
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		<item>
		<title>DOWN SYNDROME</title>
		<link>http://www.ababycare.com/down-syndrome/</link>
		<comments>http://www.ababycare.com/down-syndrome/#comments</comments>
		<pubDate>Sat, 18 Jul 2009 09:06:57 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[Down syndrome]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=167</guid>
		<description><![CDATA[
This is by far the most common of a range of conditions called trisomies, in which one pair of chromosomes has an extra chromosome, making three. In Down syndrome, there are three number 21 chromosomes. Affected infants characteristically have small features, a tongue that protrudes, and slanting eyes with folds of skin at their inner [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignnone size-full wp-image-168" title="Down syndrome " src="http://www.ababycare.com/wp-content/uploads/2009/07/baby-downs.jpg" alt="Down syndrome " width="320" height="320" /></p>
<p>This is by far the most common of a range of conditions called trisomies, in which one pair of chromosomes has an extra chromosome, making three. In Down syndrome, there are three number 21 chromosomes. Affected infants characteristically have small features, a tongue that protrudes, and slanting eyes with folds of skin at their inner corners. They tend to be rather floppy infants and have short, wide hands. They may also suffer from congenital heart disease.</p>
<p><span id="more-167"></span></p>
<p>Down syndrome babies usually mentally handicapped, though the degree of handicap varies widely; many are near normal. They are usually affectionate and happy children. With careful attention and early education, they often do very well, and some manage to live independently as adults.</p>
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		<title>CLEFT LIP AND CLEFT PALATE</title>
		<link>http://www.ababycare.com/cleft-lip-and-cleft-palate/</link>
		<comments>http://www.ababycare.com/cleft-lip-and-cleft-palate/#comments</comments>
		<pubDate>Fri, 17 Jul 2009 13:35:13 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[Cleft lip]]></category>
		<category><![CDATA[cleft palate]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=160</guid>
		<description><![CDATA[
A cleft is a split or separation of parts. During the early part of pregnancy, separate areas of the baby’s face and head develop individually, than join together. When joining does not take place or is incomplete, the baby can be born with a cleft lip on one or both sides, with or without a [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignnone size-full wp-image-164" title="Cleft lip" src="http://www.ababycare.com/wp-content/uploads/2009/07/baby-cleft-lip1.jpg" alt="Cleft lip" width="360" height="239" /></p>
<p>A cleft is a split or separation of parts. During the early part of pregnancy, separate areas of the baby’s face and head develop individually, than join together. When joining does not take place or is incomplete, the baby can be born with a cleft lip on one or both sides, with or without a cleft palate. Breastfeeding is sometimes possible, perhaps using a nipple shield; if not, special bottles and nipples are readily available. Some milk may return down the nose but this doesn’t matter.</p>
<p><span id="more-160"></span></p>
<p>A cleft lip can be surgically closed soon or some weeks after birth. The palate can be closed from about six to nine months. Further operations may be necessary for some children.</p>
<p>Affected children are looked after by a cleft-palate team which will monitor speech, hearing, and teeth and will intervene should this become necessary. Support for parents is available.</p>
]]></content:encoded>
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		<item>
		<title>CONGENITAL HEART DISEASE</title>
		<link>http://www.ababycare.com/congenital-heart-disease/</link>
		<comments>http://www.ababycare.com/congenital-heart-disease/#comments</comments>
		<pubDate>Fri, 17 Jul 2009 09:54:05 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[Congenital heart disease]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=157</guid>
		<description><![CDATA[The most common form of heart disease in newborns is a hole in the ventricular septum – the thin dividing wall between the right and left ventricles (pumping chambers). About four weeks after birth, blood will “shunt” from left to right through the hole and the oxygenated blood will flow to the lungs instead of [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignleft size-full wp-image-158" style="margin: 10px;" title="CONGENITAL HEART DISEASE" src="http://www.ababycare.com/wp-content/uploads/2009/07/1243191_Webb_Bebis_pulsoximetry.jpg" alt="CONGENITAL HEART DISEASE" width="370" height="250" />The most common form of heart disease in newborns is a hole in the ventricular septum – the thin dividing wall between the right and left ventricles (pumping chambers). About four weeks after birth, blood will “shunt” from left to right through the hole and the oxygenated blood will flow to the lungs instead of to the body. Symptoms include breathlessness, particularly during feeding. In some cases, the hole seals spontaneously, but if it doesn’t, an operation will be necessary.</p>
]]></content:encoded>
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		<item>
		<title>EPISPADIAS AND HYPOSPADIAS</title>
		<link>http://www.ababycare.com/epispadias-and-hypospadias/</link>
		<comments>http://www.ababycare.com/epispadias-and-hypospadias/#comments</comments>
		<pubDate>Fri, 17 Jul 2009 09:39:18 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[epispadias]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[hypospadias]]></category>
		<category><![CDATA[newborn baby]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=155</guid>
		<description><![CDATA[In a very small number of male babies – about 0.3 percent – there is an abnormality in the position of the urethral opening on the penis. In epispadias, the opening is on the upper surface of the penis, and the penis may curve upward; in hypospadies, the opening is on the underside of the [...]]]></description>
			<content:encoded><![CDATA[<p>In a very small number of male babies – about 0.3 percent – there is an abnormality in the position of the urethral opening on the penis. In epispadias, the opening is on the upper surface of the penis, and the penis may curve upward; in hypospadies, the opening is on the underside of the glans (head), and the penis may curve downward. In rare cases, the urethral opening lies between the genitals and the anus, and the genitals may appear to be female. Surgery can be carried out in the preschool years to correct the defect, allowing normal passage of urine and, in later life, normal sexual intercourse. Neither of these conditions, even in the severe form, causes infertility.</p>
]]></content:encoded>
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		<item>
		<title>TALIPES (CLUB FOOT)</title>
		<link>http://www.ababycare.com/talipes-club-foot/</link>
		<comments>http://www.ababycare.com/talipes-club-foot/#comments</comments>
		<pubDate>Thu, 16 Jul 2009 18:35:43 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[Club Foot]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>
		<category><![CDATA[Talipes]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=147</guid>
		<description><![CDATA[Some infants – twice as many boys as girls – are born with the sole of one or both feet facing down and inward, or up and outward. The cause of club foot is not fully understood, but it may be inherited. It may be associated with spina bifida. The foot will be manipulated over [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignleft size-full wp-image-148" style="margin: 10px;" title="TALIPES (CLUB FOOT)" src="http://www.ababycare.com/wp-content/uploads/2009/07/clubfootrepair.jpg" alt="TALIPES (CLUB FOOT)" width="229" height="171" />Some infants – twice as many boys as girls – are born with the sole of one or both feet facing down and inward, or up and outward. The cause of club foot is not fully understood, but it may be inherited. It may be associated with spina bifida. The foot will be manipulated over several months, and braced or splinted is position between manipulations. If surgery is necessary, it can be carried out when the child is as young as 12-16 weeks.</p>
]]></content:encoded>
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		<item>
		<title>CONGENITAL CONDITIONS</title>
		<link>http://www.ababycare.com/congenital-conditions/</link>
		<comments>http://www.ababycare.com/congenital-conditions/#comments</comments>
		<pubDate>Thu, 16 Jul 2009 18:31:10 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[Congenital conditions]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=145</guid>
		<description><![CDATA[Congenital handicaps are rare. Some are genetic, whereas others are due to the effects on the fetus of drugs, radiation, infections, or metabolic disturbances. The fetal tissues that are most actively growing at the time when the adverse factor operates are the ones most likely to be affected. An increasing number of defects can be [...]]]></description>
			<content:encoded><![CDATA[<p>Congenital handicaps are rare. Some are genetic, whereas others are due to the effects on the fetus of drugs, radiation, infections, or metabolic disturbances. The fetal tissues that are most actively growing at the time when the adverse factor operates are the ones most likely to be affected. An increasing number of defects can be defected before birth and successfully treated just after birth.</p>
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		<title>TUBE FEEDING</title>
		<link>http://www.ababycare.com/tube-feeding/</link>
		<comments>http://www.ababycare.com/tube-feeding/#comments</comments>
		<pubDate>Wed, 15 Jul 2009 18:08:06 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>
		<category><![CDATA[Tube Feeding]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=141</guid>
		<description><![CDATA[
Most premature and low birth-weight babies do not have the strength to suck milk from a nipple or bottle, and their intestines may be too weak to absorb food. There are three alternative ways of feeding:


Intravenous      feeding is used for babies who are very ill or so premature that they [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignnone size-full wp-image-142" title="TUBE FEEDING" src="http://www.ababycare.com/wp-content/uploads/2009/07/MON11-DSCN1280.jpg" alt="TUBE FEEDING" width="380" height="279" /></p>
<p>Most premature and low birth-weight babies do not have the strength to suck milk from a nipple or bottle, and their intestines may be too weak to absorb food. There are three alternative ways of feeding:</p>
<p><span id="more-141"></span></p>
<ul>
<li>Intravenous      feeding is used for babies who are very ill or so premature that they      cannot swallow or digest food for themselves. It may continue for weeks      and subsequent feeding will be through a stomach tube.</li>
<li>With nasogastric      feeding, a tube is passed through the baby’s nose and into the stomach or      intestine. Because the tube is very fine and soft, the baby hardly knows      it’s there, so it’s a very comfortable way to feed.</li>
<li>When      your baby is older, a combination of breast or bottle and tube feeding      will suffice; the baby feeds as much as he can from breast or bottle, and      the feeding tube supplies the rest. Combination feeding can be used once      the rooting and sucking reflexes are established and will continue until      the baby is strong enough to feed from breast or bottle only.</li>
</ul>
<p><strong>Progress</strong></p>
<p>The development of a premature baby can be slow and erratic. It is often a great shock to see just how tiny a premature baby is but he will have a great will to live.</p>
<p>For a premature baby every day can be an uphill battle. Periods of improvement may be followed by setbacks, and this constant uncertainty can make you and your partner feel anxious, moody, and restless. It is encouraging to know, however, that most babies born after 32 weeks will develop normally. Of those babies born at 27 weeks (three months early), six out of seven will survive.</p>
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		<title>BREATHING PROBLEMS</title>
		<link>http://www.ababycare.com/breathing-problems/</link>
		<comments>http://www.ababycare.com/breathing-problems/#comments</comments>
		<pubDate>Wed, 15 Jul 2009 11:40:54 +0000</pubDate>
		<dc:creator>luiza</dc:creator>
				<category><![CDATA[Newborn Health]]></category>
		<category><![CDATA[baby]]></category>
		<category><![CDATA[Breathing Problems]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[newborn]]></category>
		<category><![CDATA[newborn baby]]></category>
		<category><![CDATA[Special care babies]]></category>

		<guid isPermaLink="false">http://www.ababycare.com/?p=137</guid>
		<description><![CDATA[
A baby with respiratory distress syndrome (RDS) may stop breathing for a short time. This is called apnea. Although it sounds very frightening, apnea is not uncommon, and most babies start breathing again after gentle stimulation such as a top or a stroke. Other respiratory problems can arise from fluid inhaled into the lungs or [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignleft size-full wp-image-138" style="margin: 10px;" title="respiratory distress syndrome " src="http://www.ababycare.com/wp-content/uploads/2009/07/castro.jpg" alt="respiratory distress syndrome " width="288" height="389" /></p>
<p>A baby with respiratory distress syndrome (RDS) may stop breathing for a short time. This is called apnea. Although it sounds very frightening, apnea is not uncommon, and most babies start breathing again after gentle stimulation such as a top or a stroke. Other respiratory problems can arise from fluid inhaled into the lungs or a lack of surfactant – a substance produced in the lungs that keeps them from collapsing. If a baby’s do not have enough surfactant coating, they don’t expand as well as they should. This can cause the smaller air sacs to collapse, leading to hyaline membrane disease, a condition common in babies born before 31 weeks.</p>
<p>Babies suffering from any of these complications can be given oxygen either by way of a face mask or by a small tube inserted directly into the windpipe and attached to a ventilator.</p>
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