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Infanticide -- New York (State) -- Lansing -- Cases   2
Infanticide -- New York (State) -- New York -- Cases : The early life and complete trial of Mary, alias Polly Bodine, for the murder of Emeline Houseman and her child : containing a fac similie of her own writing, which is recorded seven different births and illustrations of hair, of her own children, which have been (as is supposed) strangled at their birth, or destroyed by abortion : together with a cut representing her as she appeared when pawning the jewelry : likewise as she appeared at trial in New-York, and at the supposed scene of arson and murder  1846 1
Infanticide -- New Zealand. : Minnie Dean : her life and crimes / Lynley Hood  1994 1
Infanticide -- Ohio -- Cincinnati -- Case studies : Driven toward madness : the fugitive slave Margaret Garner and tragedy on the Ohio / Nikki M. Taylor  2016 1
Infanticide -- Ohio -- Cincinnati -- History -- 19th century : Who speaks for Margaret Garner? / Mark Reinhardt  2010 1
Infanticide -- Press coverage : Motherhood in the Media : Infanticide, Journalism, and the Digital Age  2016 1
Infanticide -- Press coverage -- Australia -- History.   2
Infanticide -- Press coverage -- Australia -- History -- 19th century   2
Infanticide -- Press coverage -- England -- History.   2
Infanticide -- Press coverage -- England -- History -- 19th century   2
Infanticide -- Psychological aspects.   3
Infanticide -- Psychological aspects -- Case studies : Inside story. Caroline's baby / producer, Nick Catliff  1995 1
Infanticide -- psychology.   2
Infanticide -- Religious aspects. : Infanticide and the value of life / edited by Marvin Kohl  1978 1
Infanticide -- Religious aspects -- Christianity   3
Infanticide -- Religious aspects -- Christianity -- Sermons : A history of the Pocasset tragedy : with the three sermons preached in New Bedford / by William J. Potter, C.S. Nutter, and W.C. Stiles  1879 1
Infanticide -- Social aspects. : Infanticide : psychosocial and legal perspectives on mothers who kill / edited by Margaret G. Spinelli  2003 1
Infanticide -- South Carolina -- Union (Union County) : Motherhood on trial : the tragedy of Susan Smith / produced and directed by Lynn Estomin  1997 1
Infanticide -- Texas -- Houston   2
Infanticide -- United States -- Case studies   2
 

Infanticides -- See Infanticide


The killing of infants at birth or soon after
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Infantile atrophy -- See Marasmus


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  Infantile Autism -- 2 Related Subjects   2
 

Infantile Autism, Early -- See Autistic Disorder


A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V)
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Infantile Botulism -- See Botulism


A disease caused by potent protein NEUROTOXINS produced by CLOSTRIDIUM BOTULINUM which interfere with the presynaptic release of ACETYLCHOLINE at the NEUROMUSCULAR JUNCTION. Clinical features include abdominal pain, vomiting, acute PARALYSIS (including respiratory paralysis), blurred vision, and DIPLOPIA. Botulism may be classified into several subtypes (e.g., food-borne, infant, wound, and others). (From Adams et al., Principles of Neurology, 6th ed, p1208)
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Infantile Cerebral Palsy, Diplegic -- See Cerebral Palsy


A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
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Infantile Cerebral Palsy, Monoplegic -- See Cerebral Palsy


A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
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Infantile Cerebral Palsy, Quadriplegic -- See Cerebral Palsy


A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
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  Infantile Diarrhea -- 2 Related Subjects   2
 

Infantile Diarrheas -- See Diarrhea, Infantile


DIARRHEA occurring in infants from newborn to 24-months old
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Infantile Eczema -- See Dermatitis, Atopic


A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema
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Infantile Gaucher Disease -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
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Infantile Hemiplegia -- See Hemiplegia


Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body
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Infantile Hemiplegias -- See Hemiplegia


Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body
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Infantile Malnutrition -- See Infant Nutrition Disorders


Disorders caused by nutritional imbalance, either overnutrition or undernutrition, occurring in infants ages 1 month to 24 months
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Infantile myoclonic epilepsy -- See Infantile spasms


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Infantile Neuronal Ceroid Lipofuscinosis -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
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Infantile Obesity -- See Pediatric Obesity


BODY MASS INDEX in children (ages 2-12) and in adolescents (ages 13-18) that is grossly above the recommended cut-off for a specific age and sex. For infants less than 2 years of age, obesity is determined based on standard weight-for-length percentile measures
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Infantile Papular Acrodermatitides -- See Acrodermatitis


Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome
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Infantile Papular Acrodermatitis -- See Acrodermatitis


Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome
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  Infantile Paralysis -- 2 Related Subjects   2
 

Infantile Respiratory Distress Syndrome -- See Respiratory Distress Syndrome, Newborn


A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause
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Infantile Spasm -- See Spasms, Infantile


An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
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Infantile Spasm, Cryptogenic -- See Spasms, Infantile


An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
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Infantile Spasm, Symptomatic -- See Spasms, Infantile


An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
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Infantile Spasms -- See Spasms, Infantile


An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
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Infantile spasms   2
 

Infantile Spasms, Cryptogenic -- See Spasms, Infantile


An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
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Infantile spasms -- Etiology : KCNQ2- and KCNQ3-associated epilepsy / edited by Sarah Weckhuysen, Alfred L. George  2022 1
Infantile spasms -- Genetic aspects : KCNQ2- and KCNQ3-associated epilepsy / edited by Sarah Weckhuysen, Alfred L. George  2022 1
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