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Glossary for Inverted nipple/nipple retraction

Medical terms related to Inverted nipple/nipple retraction or mentioned in this section include:

  • 2q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Behavioral symptoms: Symptoms of personal behavior.
  • Body symptoms: Symptoms affecting the entire body features.
  • Breast Feeding: Nursing an infant with breast milk.
  • Breast abscess: The presence of an abscess which has formed within the breast
  • Breast carcinoma: Carcinoma occurring in breast tissue.
  • Breast lump: Lump in the breast or on the skin area
  • Breast symptoms: Any symptom affecting one or both breasts.
  • CDG syndrome (generic term): Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. The main symptom in all the disorders is psychomotor retardation but other variable symptoms also occur depending on the subtype of the disorder.
  • CDG syndrome type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Chromosome 2, monosomy 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Congenital Disorders of Glycosylation Type Ia: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Congenital disorder of glycosylation type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Congenital disorder of glycosylation type 1L: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Il is caused by a defect on chromosome 11q23 and involves a defect in the ALG9 gene.
  • Deletion 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Developmental problems: Physical or mental development difficulty.
  • Duane Syndrome: An inherited eye movement disorder. The eye opening narrows and the eyeball pulls backwards when the eyes look towards the nose.
  • Face symptoms: Symptoms affecting the face
  • Fryns-Aftimos syndrome: A rare syndrome characterized mainly by abnormal brain development, epilepsy, mental retardation and unusual facial appearance.
  • Head symptoms: Symptoms affecting the head or brain
  • Holoprosencephaly, recurrent infections, and monocytosis: A rare syndrome characterized by recurring infections and a brain anomaly. Death usually occurs during the first years of life due to sepsis.
  • Hypotonia, Seizures and Precocious Puberty: A rare syndrome observed in three siblings and characterized mainly by seizures and reduced muscle tone. Early puberty was also observed in two of the children.
  • Inflammatory breast cancer: Inflammatory breast cancer is a rare and aggressive form of invasive breast cancer, where the skin of the breast becomes red, inflamed and pitted in appearance.
  • Injury: Any damage inflicted in the body
  • Kennerknecht syndrome: A very rare syndrome characterized mainly by absent gonads, mental retardation, short stature, retarded bone age and heart abnormalities. The observed cases involved a family whose parents were related.
  • Kennerknecht-Sorgo-Oberhoffer syndrome: A very rare syndrome characterized mainly by absent gonads and an underdeveloped right side of the heart.
  • Mastitis: Infected breast common in nursing mothers
  • Nerve symptoms: Symptoms affecting the nerves
  • Nipple abnormality: Abnormality in the sensation, texture or appearance of the nipples, or unusual associated symptoms such as bleeding or discharge
  • Nipple conditions: Any condition that affects the nipples
  • Nipple lump: Lump felt in or behind the nipple
  • Nipple pain: Nipple pain is discomfort in a nipple.
  • Nipple retraction: Nipple retraction is a condition in which a nipple has withdrawn into the breast tissue.
  • Nipple symptoms: Any symptom affecting the nipple.
  • Swelling symptoms: Symptoms causing swelling or enlargement.
  • Weaver Syndrome: A syndrome that is considered a variant of the Marshall-Smith syndrome

Conditions listing medical symptoms: Inverted nipple/nipple retraction:

The following list of conditions have 'Inverted nipple/nipple retraction' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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