Microcephaly is a neurological condition where an infant's head is significantly smaller than a healthy child's head.
Mikrosefali bebeğin başının sağlıklı bir çocuğun başını daha küçük olan bir nörolojik durumdur.
Kaynak: ibtimes.co.uk Dubowitz syndrome is a rare genetic disorder characterized by
microcephaly , growth retardation and a characteristic facial appearance
Kaynak: Dubowitz syndromeHalal syndrome is a rare disorder characterised by
microcephaly , cleft palate , and variable other anomalies. References : of
microcephalyKaynak: Halal syndromeMirhosseini–Holmes–Walton syndrome is a syndrome which involves retinal degeneration , cataract ,
microcephaly , and mental retardation .
Kaynak: Mirhosseini–Holmes–Walton syndromeMukamel syndrome is a cutaneous condition characterized by premature graying, lentigines, depigmented macules,
microcephaly, and scoliosis
Kaynak: Mukamel syndromeMental retardation and
microcephaly with pontine and cerebellar hypoplasia. 300749 CASK Mental retardation in cri-du-chat syndrome
Kaynak: List of OMIM disorder codesautosomal recessive genetic disorder, consisting of a variety of features including hiatal hernia ,
microcephaly and nephrotic syndrome
Kaynak: Galloway Mowat syndromeChiari malformation , lissencephaly , and
microcephaly Although the exact cause of colpocephaly is not known yet, it is commonly believed
Kaynak: ColpocephalyThe clinical features include small hands and feet and a deceleration of the rate of head growth (including
microcephaly in some).
Kaynak: Rett syndromeunder The Killers of Comedy Tour banner Beetle also has an extreme difficulty in repeating simple phrases, presumably due to his
microcephaly .
Kaynak: Beetlejuice (entertainer)Other physical abnormalities associated with this disorder can include an unusually small head (
microcephaly ), and malformations of the
Kaynak: Lenz microphthalmia syndromeA person with
microcephaly , in freak show s promoted as "human pinheads. "List of disability-related terms with negative connotations
Kaynak: PinheadMutations in this gene are associated with Seckel syndrome and primary autosomal recessive
microcephaly , a disorder characterized by
Kaynak: CENPJgrowth retardation,
microcephaly, and immunodeficiency The protein is required for the non-homologous end joining (NHEJ) pathway of DNA repair .
Kaynak: XLF (protein)