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  • Spina bifida

    Read about spina bifida, which is a condition where an unborn baby's spine and spinal cord does not develop properly.

  • Prader-Willi syndrome

    Find out about Prader-Willi syndrome (PWS), which is a rare genetic condition that causes a wide range of physical symptoms, learning difficulties and behavioural challenges.

  • 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.

  • Muscular dystrophy

    The muscular dystrophies (MD) are a group of inherited genetic conditions that gradually cause the muscles to weaken, leading to an increasing level of disability.

  • Medicines information

    As medicines are a crucial part of medical treatment, it's important to have a good understanding of them.

  • Lost or changed sense of smell

    A change in your sense of smell can be unpleasant and affect how things taste. But it's not usually serious and may get better in a few weeks or months.

  • 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.