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Fetal minoxidil syndrome

Disease definition

Fetal minoxidil syndrome is characterized by a group of symptoms that may be observed in a fetus or newborn when the mother has taken minoxidil during pregnancy. Minoxidil is used in the treatment of malignant renal hypertension and as a topical solution to induce scalp hair growth. Hypertrichosis that gradually diminishes during the first six postnatal months has been reported. Additional reported features include cardiac (congenital great vessel transposition and pulmonary valve stenosis), neurodevelopmental (caudal regression sequence) (see these terms), gastrointestinal, renal, and limb malformations. Conclusive studies are however not available.

ORPHA:1918

Classification level: Disorder
  • Synonym(s):
    • Minoxidil antenatal exposure
  • Prevalence: Unknown
  • Inheritance: Not applicable 
  • Age of onset: Antenatal, Neonatal
  • ICD-10: Q86.8
  • ICD-11: LD2F.0Y
  • OMIM: -
  • UMLS: C0432373
  • MeSH: -
  • GARD: 2308
  • MedDRA: -

  A summary on this disease is available in Español (2016) Italiano (2016) Nederlands (2016) Français (2005) Deutsch (2005)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.