Keratolysis Exfoliativa Congenita
Keratolysis exfoliativa congenita is a rare skin disorder characterized by superficial peeling of the skin of the palms and soles in the absence of inflammation.
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Kenny Disease
Kenny Disease is a very rare inherited skeletal disorder involving thickening of the long bones of the body and with the abnormalities of the head.
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XO Syndrome
XO syndrome or
Turner syndrome or Ulrich Turner syndrome is also known as
gonadal dysgenesis is a group of conditions in which
X chromosome shows monosomy or in other words one X chromosome is entirely deleted or may be partly deleted. It is a type of chromosomal disorder in which sex chromosomes are affected.
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XYY Chromosome Pattern
XYY Chromosome pattern is an rare chromosomal abnormality that is affecting males characterized by an extra copy of Y Chromosome ( 47 XYY).
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XLP
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XXXXX Syndrome
49, XXXXX chromosome or XXXXX syndrome is also known as pentasomy X. This syndrome is characterised by the presence of three additional X chromosomes. Only way to diagnose the condition is by karyotyping.
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Septal perforations
Septal perforation is a hole in the
nasal septum, the tissue that separates the nostrils. It can occur as a result of previous nasal surgery or as a result of
nasal fracture. It can also occur after long term use of cocaine.
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RosaiDorfman Disease
This is also known as
sinus histiocytosis with massive
lymphadenopathy. It is a rare and benign disorder. The etiology of this disease is not known. It is characterized by formation of increased production of histiocytes which accumulate in lymph nodes throughout the body.
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Pulmonary Eosinophilia
Pulmonary
Eosinophilia is inflammation of the lungs associated with an increase in blood or tissue esinophils. Eosinophilia is due to extrinsic or intrinsic factors. Symptoms range from none at all to severe.
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Impotent Neutrophil Syndrome
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