Copper deficiency (Q39940): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Deficiência dietética é rara e tem sido observada em prematuros e bebês com baixo peso ao nascimento que são alimentados exclusivamente com leite de vaca e em indivíduos em nutrição parenteral total (NPT) prolongada sem cobre. Manifestações clínicas incluem despigmentação de pele e cabelo, distúrbios neurológicos, leucopenia, anemia microcítica e hipocrômica e anormalidades esqueléticas.
@@ description / en / description / en @@
+Dietary deficiency is rare; it has been observed in premature and low birthweight infants fed exclusively a cow’s milk diet and in individuals on long-term total parenteral nutrition without copper. Clinical manifestations include depigmentation of skin and hair, neurologic disturbances, leukopenia, hypochromic microcytic anaemia, and skeletal abnormalities.
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
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@@ Property / Collection date: 13 August 2026 / rank @@
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@@ Property / Linked ICD 10 @@
+E61.0
@@ Property / Linked ICD 10: E61.0 / rank @@
+Normal rank

Latest revision as of 05:33, 13 August 2026

Dietary deficiency is rare; it has been observed in premature and low birthweight infants fed exclusively a cow’s milk diet and in individuals on long-term total parenteral nutrition without copper. Clinical manifestations include depigmentation of skin and hair, neurologic disturbances, leukopenia, hypochromic microcytic anaemia, and skeletal abnormalities.

Language	Label	Description	Also known as
default for all languages	5B5K.6
English	Copper deficiency	Dietary deficiency is rare; it has been observed in premature and low birthweight infants fed exclusively a cow’s milk diet and in individuals on long-term total parenteral nutrition without copper. Clinical manifestations include depigmentation of skin and hair, neurologic disturbances, leukopenia, hypochromic microcytic anaemia, and skeletal abnormalities.