PubMedID: 18465422A 7-month-old baby was born in a village near Iskenderun (Turkey) where "Unertan Syndrome" with quadrupedality and primitive cognitive abilities was discovered. The clinical diagnosis was anencephaly. However, his head did not show the classical symptoms of anencephaly because it was covered with bony structures. The baby has an ape-like, prognasthic head with low-set ears and flapped ear flaps. The other parts of the body were similar to humans with broad shoulders and a short neck. This may be a further example of human devolution, which was first reported by Tan (2005, 2006a,b,c). A genetic defect affecting the head development including brain may be responsible for the reappearance of the ape-like head in a human being...
Craniorachischisis is the most severe type of neural tube defect in which almost the entire brain an...
PubMedID: 16861146A new family exhibiting "Unertan Sydnrome" was discovered. The pedigree analysis s...
The camptomelic syndrome is characterised by neonate dwarfism of micromelic type with multiple anoma...
PubMedID: 18205078The aim of this study was to describe additional patients (n= 3) exhibiting the Un...
A large family with six individuals exhibiting the Unertan syndrome (UTS) was identified residing in...
Anencephaly is one of the most frequent type of all fetal mon-strosities. Sprangler7, who studied 11...
Iniencephaly is form of neural tube defect which includes occipital bone defect at foramen magnum al...
The aim of this study was to describe additional patients (n = 3) exhibiting the Unertan syndrome (U...
The aim of this study was to describe additional patients (n = 3) exhibiting the Unertan syndrome (U...
Anencephaly which is basically a misnomer used in place of meroencephaly for a long time is one of t...
Virginia. This is, she was born missing almost all of her brain. In fact, all that remained of her b...
Iniencephaly is a rare and fatal neural tube defect characterized by retroflexion of fetal head with...
PubMedID: 18300005"Unertan syndrome" consists of two main symptoms: quadrupedal gait and primitive c...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
We offer further biological characterization of the XK atelen/ aprosencephaly syndrome in two infant...
Craniorachischisis is the most severe type of neural tube defect in which almost the entire brain an...
PubMedID: 16861146A new family exhibiting "Unertan Sydnrome" was discovered. The pedigree analysis s...
The camptomelic syndrome is characterised by neonate dwarfism of micromelic type with multiple anoma...
PubMedID: 18205078The aim of this study was to describe additional patients (n= 3) exhibiting the Un...
A large family with six individuals exhibiting the Unertan syndrome (UTS) was identified residing in...
Anencephaly is one of the most frequent type of all fetal mon-strosities. Sprangler7, who studied 11...
Iniencephaly is form of neural tube defect which includes occipital bone defect at foramen magnum al...
The aim of this study was to describe additional patients (n = 3) exhibiting the Unertan syndrome (U...
The aim of this study was to describe additional patients (n = 3) exhibiting the Unertan syndrome (U...
Anencephaly which is basically a misnomer used in place of meroencephaly for a long time is one of t...
Virginia. This is, she was born missing almost all of her brain. In fact, all that remained of her b...
Iniencephaly is a rare and fatal neural tube defect characterized by retroflexion of fetal head with...
PubMedID: 18300005"Unertan syndrome" consists of two main symptoms: quadrupedal gait and primitive c...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
We offer further biological characterization of the XK atelen/ aprosencephaly syndrome in two infant...
Craniorachischisis is the most severe type of neural tube defect in which almost the entire brain an...
PubMedID: 16861146A new family exhibiting "Unertan Sydnrome" was discovered. The pedigree analysis s...
The camptomelic syndrome is characterised by neonate dwarfism of micromelic type with multiple anoma...