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  • Oesophageal atresia and tracheo-oesophageal fistula

    Oesophageal atresia is a rare birth defect that affects a baby's oesophagus (the tube through which food passes from the mouth to the stomach).

  • Noonan syndrome

    Read about Noonan syndrome, which is a genetic disorder that causes a wide range of features, such as heart abnormalities and unusual facial features.

  • Myasthenia gravis

    Read about myasthenia gravis, including the symptoms and when to see a GP. Also, find out what causes the condition, how it's treated and the outlook.

  • Idiopathic pulmonary fibrosis

    Find out about idiopathic pulmonary fibrosis (IPF), including what the symptoms are, how it's treated and what the outlook is.

  • Hereditary spastic paraplegia

    Find out about hereditary spastic paraplegia (HSP), a rare group of inherited disorders that often cause weakness and stiffness in the leg muscles, which gradually gets worse over time.

  • Frontotemporal dementia

    Find out what frontotemporal dementia is, what the symptoms are, how it's treated, and what the outlook is.

  • Congenital heart disease

    Find out about the different types of congenital heart disease, why it happens, the signs and symptoms and how it's treated.

  • Charcot-Marie-Tooth disease

    Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that cause nerve damage, leading to muscle weakness and numbness

  • Angelman syndrome

    Read about Angelman syndrome, a genetic disorder that affects the nervous system and causes severe physical and intellectual disability

  • Androgen insensitivity syndrome

    Find out about androgen insensitivity syndrome (AIS), a rare condition that affects the development of a person's genitals and reproductive organs.