retraso en el desarrollo

dolor de cabeza, problemas de visión, una mala coordinación, vómitos

Hydrocephalus, sometimes known as Water on the Brain, is a condition in which abnormal accumulation of cerebrospinal fluid (CSF) in the brain causes increased intracranial pressure inside the skull. This is usually due to blockage of CSF outflow in the brain ventricles or in the subarachnoid space at the base of the brain. ... 

debilidad, debilidad muscular en el pie pies, debilidad muscular en las piernas, dificultad para caminar

bajo tono muscular, frecuentes caídas, movimientos anormales, pasando a cabo

Lennox-Gastaut syndrome (LGS), also known as Lennox syndrome, is a difficult-to-treat form of childhood-onset epilepsy that most often appears between the second and sixth year of life, and is characterized by frequent seizures and different seizure types; it is often accompanied by mental retardation and behavior problems ... 

cambios de comportamiento, convulsiones, retraso en el desarrollo, una mala coordinación

The diagnostic category pervasive developmental disorders (PDD), as opposed to specific developmental disorders (SDD), refers to a group of five disorders characterized by delays in the development of multiple basic functions including socialization and communication. The most commonly known PDD is (1) Autism, with the remaining identified as (2) Rett syndrome, (3) Childhood disintegrative disorder, (4) Asperger syndrome, and (5) Pervasive Developmental Disorder Not Otherwise Specified (or PDD-NOS). ... 

ampollas o golpes en los pies, enrojecimiento a pie pies, enrojecimiento de los dedos de los pies, la limitación de movimiento

Renal osteodystrophy is a bone pathology, characterized by defective mineralization, that results from renal disease. renal - refers to kidney, osteo - refers to bone, and dystrophy - means degenerative disorder (like dystrophy in muscular dystrophy). ... 

diarrea, fiebre, retraso en el desarrollo, tos

CVID is believed to be a genetically determined primary immune defect; however, the underlying causes are different. The result of these defects is that the patient doesn't produce sufficient antibodies in response to exposure to pathogens. As a result, the patient's immune system fails to protect them against common bacterial and viral (and occasionally parasitic and protozoal) infections. The net result is that the patient is prone to illness. Both parts of the immune system (the cellular and humoral system) are affected, hence its classification as a combined immunodeficiency. ... 

inquietud, no aumentar de peso, problemas de aprendizaje, retraso en el desarrollo

Fetal alcohol syndrome or FAS is a disorder of permanent birth defects that occurs in the offspring of women who drink alcohol during pregnancy. It is unknown whether amount, frequency or timing of alcohol consumption during pregnancy causes a difference in amount of damage done to the fetus. Thus, the current recommendation is not to drink at all during pregnancy. Alcohol crosses the placental barrier and can stunt fetal growth or weight, create distinctive facial stigmata, damage neurons and brain structures, and cause other physical, mental, or behavioral problems. ... 

convulsiones, dificultad para caminar, la limitación de movimiento, parálisis

Cerebral palsy (CP) is a umbrella term encompassing a group of non-progressive, non-contagious neurological disorders that cause physical disability in human development, specifically the human movement and posture. ... 

erupción, fotofobia, retraso en el desarrollo, temblor

Hartnup disease, or Hartnup's disease, or Hartnup disorder, is an autosomal resssive genetic metabolic disorder in the absorption of the amino acidtryptophan that can be, in turn, converted into Serotonin, Melatonin and Niacin. Niacin is a precursor to nicotinamide, a necessary component of NAD+. ... 

abultamientos en la piel, ampollas o golpes en la espalda, café au lait spots, dolor pélvico

Neurofibromatosis type I (NF-1), also known as von Recklinghausen syndrome, comprises, along with neurofibromatosis type II (a.k.a. MISME syndrome), tuberous sclerosis, Sturge-Weber, and Von Hippel-Lindau disease, the phakomatoses or neurocutaneous syndromes, all of which have both neurologic and dermatologic lesions. This grouping is an artifact of an earlier time in medicine, before the distinct genetic basis of each of these disorders was understood. ...