Cholestasis - lymphoedema syndrome (Q64269)

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Cholestasis-lymphoedema syndrome is characterised by chronic severe lymphoedema and severe neonatal cholestasis that usually lessens during early childhood and becomes episodic. It has been described in six large families, mainly from Norway. The common feature of this autosomal recessive condition is a generalised lymphatic anomaly.
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    Cholestasis - lymphoedema syndrome
    Cholestasis-lymphoedema syndrome is characterised by chronic severe lymphoedema and severe neonatal cholestasis that usually lessens during early childhood and becomes episodic. It has been described in six large families, mainly from Norway. The common feature of this autosomal recessive condition is a generalised lymphatic anomaly.

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