Silver–Russell dwarfism also called Silver–Russell syndrome (SRS) or Russell–Silver syndrome (RSS) is a growth disorder occurring in approximately 1/50000 to 1/100000 births. In the United States it is usually referred […]
List of articles in "Disease" category - Page 53
Shwachman–Diamond syndrome
Shwachman–Diamond syndrome (SDS) or Shwachman–Bodian–Diamond syndrome is a rare congenital disorder characterized by exocrine pancreatic insufficiency bone marrow dysfunction skeletal abnormalities and short stature. After cystic fibrosis (CF) it is […]
Halogenoderma
Halogenodermas are skin eruptions that result after exposure to halogen-containing drugs or substances. This may last several weeks after drug use is discontinued. This is because of the slow elimination […]
Laryngoonychocutaneous syndrome
Shabbir syndrome (also known as Laryngo–onycho–cutaneous syndrome) is a cutaneous condition inherited in an autosomal recessive fashion.It was characterized by Shabbir in 1986.It may be associated with LAMA3.
Senile pruritus
Senile pruritus is a term occasionally used to refer to idiopathic itch in the elderly.
Kraurosis vulvae
Kraurosis vulvae is a cutaneous condition characterized by atrophy and shrinkage of the skin of the vagina and vulva often accompanied by a chronic inflammatory reaction in the deeper tissues.
Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome
Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome (also known as KLICK syndrome) is a cutaneous condition characterized by ichthyosis and keratoderma.It is associated with POMP.
Neonatal sepsis
In common clinical usage neonatal sepsis specifically refers to the presence in a newborn baby (neonate) of a bacterial blood stream infection (BSI) (such as meningitis pneumonia pyelonephritis or gastroenteritis) […]
Congenital cytomegalovirus infection
Congenital cytomegalovirus infection refers to a condition where cytomegalovirus is transmitted in the perinatal period.HCMV is one of the TORCH infections that lead to congenital abnormalities. (These are: toxoplasmosis rubella […]
Craniosynostosis–anal anomalies–porokeratosis syndrome
Craniosynostosis–anal anomalies–porokeratosis syndrome (also known as CAP syndrome) is a cutaneous condition inherited in an autosomal recessive fashion.