Search results for NHS UK: Rare Genetic Conditions and Developmental Delays in Children.

361 - 370 of 2007 results for "NHS UK: Rare Genetic Conditions and Developmental Delays in Children."

• Viewing or changing your GP surgery – NHS App help

  How to view or change your GP surgery using the NHS App.

• Noonan syndrome

  Find out about Noonan syndrome, including what problems it can cause, how it happens, how it's diagnosed, and the treatment and support available.

• About cefalexin

  NHS medicines information on cefalexin – what it's used for and key facts.

• Androgen insensitivity syndrome - Causes

  The genetic alteration that causes androgen insensitivity syndrome means the body cannot respond to testosterone properly.

• Viewing allergies and adverse reactions – NHS App help

  Find out how to view your allergies and adverse reactions in the NHS App.

• Viewing or changing your home address – NHS App help

  How to view or change your home address using the NHS App.

• Taking co-codamol for children with other medicines and herbal supplements

  NHS medicines information on possible interactions with co-codamol and other medicines, herbal remedies and supplements.

• Hydroxychloroquine

  NHS information about the medicine hydroxychloroquine, including what it's used for, who can use it, how to use it and side effects.

• Omeprazole: a medicine to treat heartburn and indigestion

  NHS information about the medicine omeprazole, including what it's used for, who can take it, how to take it and side effects.

• 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.